281 Writing Intern jobs in the United States
Writing Center Assistant & Writing Tutor
14651 Rochester, New York
University of Rochester
Posted today
Job Viewed
Job Description
As a community, the University of Rochester is defined by a deep commitment to Meliora - Ever Better. Embedded in that ideal are the values we share: equity, leadership, integrity, openness, respect, and accountability. Together, we will set the highest standards for how we treat each other to ensure our community is welcoming to all and is a place where all can thrive.
**Job Location (Full Address):**
755 Library Rd, Room G122, Rochester, New York, United States of America, 14627
**Opening:**
Worker Subtype:
Regular
Time Type:
Full time
Scheduled Weekly Hours:
35
Department:
Writing, Speaking, and Argument
Work Shift:
UR - Day (United States of America)
Range:
UR URG 104 H
Compensation Range:
$18.65 - $26.11
_The referenced pay range represents the minimum and maximum compensation for this job. Individual annual salaries/hourly rates will be set within the job's compensation range, and will be determined by considering factors including, but not limited to, market data, education, experience, qualifications, expertise of the individual, and internal equity considerations._
**Responsibilities:**
GENERAL SUMMARY
With minimum direction and considerable latitude for initiative and judgment, the Administrative Coordinator III is an active member of the Writing, Speaking, and Argument Program, providing secretarial support to the program. Serves as a writing consultant, tutoring undergraduate and graduate students, and acts as an assistant to the Writing and Speaking Center Director. Assists with various projects, organizes a variety of events, and provides backup to other support staff as needed. This position has the possibility of one remote working day per week.
ADMINISTRATIVE COORDINATOR III (H)
Salary Grade 009
Full Time
12-month position
35 hours per week
9:00 am - 5:00 pm
**Specific Responsibilities**
**30% Provides Writing Tutoring -** Will provide approximately 10 hours of writing tutoring in the Writing and Speaking Center weekly during the academic year.
**30%** **Secretary/Receptionist** **-** Serves as a program secretary/receptionist; triages phone calls; sorts and routes mail; maintains and purchases office supplies; assists with maintenance and service calls for the program's two copiers, fax machine, and printers; assists with overall maintenance and organization of office space. Responsible for copying, faxing, and scanning documents. Assists administrative assistant and secretary IV as needed with paperwork related to program operations including pay invoices, request for payments, and employee expense reports. Provides cross-coverage in shared clerical office and assists with general office needs including maintaining contact information, library inventory, scheduling rooms as needed, proofreading and editing as required.
**20% Supports the Writing and Speaking Center (WSC) -** Assists in the day-to-day operation of the Writing and Speaking Center. This involves working with staff to manage the consulting schedule, creating standing appointments, monitoring shift changes, ensuring that the WSAP webpage contains accurate information about WSC, assisting with proofreading and sending of session summary forms, and facilitating the distribution of consultant evaluation surveys. Coordinates and performs informational class visits about WSC resources and collects WSC usage data weekly. Also, will assist with Writing Center consultant and fellow development including supporting recruitment and training courses, making decisions about what kinds of workshops tutors may need, coordinating these workshops, and making decisions to help students with special needs around tutoring. Supports undergraduate Writing Fellows as needed. Organizes and helps to build a sense of community among alumni who were part of the WSAP.
**20% Event Management -** Organizes WSAP's special events including the annual Undergraduate Writing Colloquium Contest and UR Night to Write, creating posters, coordinating publicity, reserving space, etc. Assists in organization of awards ceremonies, Writing Fellows' Write-a-thon, WSAP Orientation Meeting in late August, Fall Kick-Off Party, and other events as scheduled. Assists the Graduate Writing Project on various tasks related to their programming such as writing boot camps and workshops. Supports faculty with clerical tasks. Updates website content and announcements.
**Preferred Qualifications**
+ Bachelor's degree.
+ At least one year of experience tutoring students in either written or spoken communication.
+ The individual in this position must have good judgment and strong customer-relations skills, be an assertive problem-solver and team player with the ability to adjust to changing priorities and challenges in a busy environment.
+ Excellent organizational, interpersonal problem-solving, and written and spoken communication skills. Experience working with students and a background in writing tutoring desirable. Advanced skills in Microsoft Office are preferred.
The University of Rochester is committed to fostering, cultivating, and preserving an inclusive and welcoming culture to advance the University's Mission to Learn, Discover, Heal, Create - and Make the World Ever Better. In support of our values and those of our society, the University is committed to not discriminating on the basis of age, color, disability, ethnicity, gender identity or expression, genetic information, marital status, military/veteran status, national origin, race, religion, creed, sex, sexual orientation, citizenship status, or any other characteristic protected by federal, state, or local law (Protected Characteristics). This commitment extends to non-discrimination in the administration of our policies, admissions, employment, access, and recruitment of candidates, for all persons consistent with our values and based on applicable law.
Notice: If you are a **Current** **Employee,** please **log into myURHR** to search for and apply to jobs using the Jobs Hub. Your application, if submitted using this portal, cannot be moved forward.
**Learn. Discover. Heal. Create.**
Located in western New York, Rochester is our namesake and our home. One of the world's leading research universities, Rochester has a long tradition of breaking boundaries-always pushing and questioning, learning and unlearning. We transform ideas into enterprises that create value and make the world ever better.
If you're looking for a career in higher education or health care, the University of Rochester may offer the perfect opportunity for your background and goals
At the University of Rochester, we are committed to fostering, cultivating, and preserving an inclusive and welcoming culture and are united by a strong commitment to be ever better-Meliora. It is an ideal that informs our shared mission to ensure all members of our community feel safe, respected, included, and valued.
**Job Location (Full Address):**
755 Library Rd, Room G122, Rochester, New York, United States of America, 14627
**Opening:**
Worker Subtype:
Regular
Time Type:
Full time
Scheduled Weekly Hours:
35
Department:
Writing, Speaking, and Argument
Work Shift:
UR - Day (United States of America)
Range:
UR URG 104 H
Compensation Range:
$18.65 - $26.11
_The referenced pay range represents the minimum and maximum compensation for this job. Individual annual salaries/hourly rates will be set within the job's compensation range, and will be determined by considering factors including, but not limited to, market data, education, experience, qualifications, expertise of the individual, and internal equity considerations._
**Responsibilities:**
GENERAL SUMMARY
With minimum direction and considerable latitude for initiative and judgment, the Administrative Coordinator III is an active member of the Writing, Speaking, and Argument Program, providing secretarial support to the program. Serves as a writing consultant, tutoring undergraduate and graduate students, and acts as an assistant to the Writing and Speaking Center Director. Assists with various projects, organizes a variety of events, and provides backup to other support staff as needed. This position has the possibility of one remote working day per week.
ADMINISTRATIVE COORDINATOR III (H)
Salary Grade 009
Full Time
12-month position
35 hours per week
9:00 am - 5:00 pm
**Specific Responsibilities**
**30% Provides Writing Tutoring -** Will provide approximately 10 hours of writing tutoring in the Writing and Speaking Center weekly during the academic year.
**30%** **Secretary/Receptionist** **-** Serves as a program secretary/receptionist; triages phone calls; sorts and routes mail; maintains and purchases office supplies; assists with maintenance and service calls for the program's two copiers, fax machine, and printers; assists with overall maintenance and organization of office space. Responsible for copying, faxing, and scanning documents. Assists administrative assistant and secretary IV as needed with paperwork related to program operations including pay invoices, request for payments, and employee expense reports. Provides cross-coverage in shared clerical office and assists with general office needs including maintaining contact information, library inventory, scheduling rooms as needed, proofreading and editing as required.
**20% Supports the Writing and Speaking Center (WSC) -** Assists in the day-to-day operation of the Writing and Speaking Center. This involves working with staff to manage the consulting schedule, creating standing appointments, monitoring shift changes, ensuring that the WSAP webpage contains accurate information about WSC, assisting with proofreading and sending of session summary forms, and facilitating the distribution of consultant evaluation surveys. Coordinates and performs informational class visits about WSC resources and collects WSC usage data weekly. Also, will assist with Writing Center consultant and fellow development including supporting recruitment and training courses, making decisions about what kinds of workshops tutors may need, coordinating these workshops, and making decisions to help students with special needs around tutoring. Supports undergraduate Writing Fellows as needed. Organizes and helps to build a sense of community among alumni who were part of the WSAP.
**20% Event Management -** Organizes WSAP's special events including the annual Undergraduate Writing Colloquium Contest and UR Night to Write, creating posters, coordinating publicity, reserving space, etc. Assists in organization of awards ceremonies, Writing Fellows' Write-a-thon, WSAP Orientation Meeting in late August, Fall Kick-Off Party, and other events as scheduled. Assists the Graduate Writing Project on various tasks related to their programming such as writing boot camps and workshops. Supports faculty with clerical tasks. Updates website content and announcements.
**Preferred Qualifications**
+ Bachelor's degree.
+ At least one year of experience tutoring students in either written or spoken communication.
+ The individual in this position must have good judgment and strong customer-relations skills, be an assertive problem-solver and team player with the ability to adjust to changing priorities and challenges in a busy environment.
+ Excellent organizational, interpersonal problem-solving, and written and spoken communication skills. Experience working with students and a background in writing tutoring desirable. Advanced skills in Microsoft Office are preferred.
The University of Rochester is committed to fostering, cultivating, and preserving an inclusive and welcoming culture to advance the University's Mission to Learn, Discover, Heal, Create - and Make the World Ever Better. In support of our values and those of our society, the University is committed to not discriminating on the basis of age, color, disability, ethnicity, gender identity or expression, genetic information, marital status, military/veteran status, national origin, race, religion, creed, sex, sexual orientation, citizenship status, or any other characteristic protected by federal, state, or local law (Protected Characteristics). This commitment extends to non-discrimination in the administration of our policies, admissions, employment, access, and recruitment of candidates, for all persons consistent with our values and based on applicable law.
Notice: If you are a **Current** **Employee,** please **log into myURHR** to search for and apply to jobs using the Jobs Hub. Your application, if submitted using this portal, cannot be moved forward.
**Learn. Discover. Heal. Create.**
Located in western New York, Rochester is our namesake and our home. One of the world's leading research universities, Rochester has a long tradition of breaking boundaries-always pushing and questioning, learning and unlearning. We transform ideas into enterprises that create value and make the world ever better.
If you're looking for a career in higher education or health care, the University of Rochester may offer the perfect opportunity for your background and goals
At the University of Rochester, we are committed to fostering, cultivating, and preserving an inclusive and welcoming culture and are united by a strong commitment to be ever better-Meliora. It is an ideal that informs our shared mission to ensure all members of our community feel safe, respected, included, and valued.
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0
Proposal Specialist - Writing
63461 Palmyra, Missouri
Insight Global
Posted today
Job Viewed
Job Description
Job Description
Insight Global is looking for a Proposal Specialist for one of the largest telecom companies in the nation. This individual will be supporting the sales team and enhancing the sales cycle by reviewing RFPs and bids from local and state governments and educational institutions who are seeking telecommunication services and coordinating and responding to bids. The Proposal Specialist must read and understand solicitation documents, meet with stakeholders (billing, finance, product, etc.) to dissect the bids, and create/write the full proposals from scratch with unique content. They will follow up with various teams and coordinate with stakeholders to get appropriate signatures. They will be responsible for providing status updates and metrics for the sales team to leverage. This job will be performed fully on-site in Ballwin, MO. Pay Rate is between 20-25/hr.
We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy:
Skills and Requirements
1+ years of experience with creative or technical writing
Extensive experience with Microsoft Suite
Professional or creative or technical writing experience null
We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal employment opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment without regard to race, color, ethnicity, religion,sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military oruniformed service member status, or any other status or characteristic protected by applicable laws, regulations, andordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or the recruiting process, please send a request to
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1
Proposal Specialist - Writing
Manchester, Missouri
Insight Global
Posted 8 days ago
Job Viewed
Job Description
Job Description
Insight Global is looking for a Proposal Specialist for one of the largest telecom companies in the nation. This individual will be supporting the sales team and enhancing the sales cycle by reviewing RFPs and bids from local and state governments and educational institutions who are seeking telecommunication services and coordinating and responding to bids. The Proposal Specialist must read and understand solicitation documents, meet with stakeholders (billing, finance, product, etc.) to dissect the bids, and create/write the full proposals from scratch with unique content. They will follow up with various teams and coordinate with stakeholders to get appropriate signatures. They will be responsible for providing status updates and metrics for the sales team to leverage. This job will be performed fully on-site in Ballwin, MO. Pay Rate is between 20-25/hr.
We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy:
Skills and Requirements
1+ years of experience with creative or technical writing
Extensive experience with Microsoft Suite
Professional or creative or technical writing experience null
We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal employment opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment without regard to race, color, ethnicity, religion,sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military oruniformed service member status, or any other status or characteristic protected by applicable laws, regulations, andordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or the recruiting process, please send a request to
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2
Content Writing Intern
22350 Alexandria, Virginia
KME Digital
Posted 10 days ago
Job Viewed
Job Description
As a KME.digital Content Writing Intern, you will write and edit marketing content, particularly blogs and website copy, for numerous businesses. You will also collaborate with our close-knit team to ensure every piece of content meets clients' goals. This job offers a breadth of experience to budding writers and creative types.
Responsibilities:
- Keep up with industry news, knowledge, and best practices
- Regularly produce various types of content, including blogs, SEO and service pages, email blasts, and newsletters
- Assist in the research, development, and curation of content ideas
- Identify opportunities for content promotion
- Provide Search Engine Optimization (SEO) support
- Assist with content marketing campaigns to drive leads and subscribers
- Utilize SEO best practices to generate traffic for a client's website
- Proofread and edit content produced by other members of the team
- Collaborate with other departments to create innovative content ideas
- Outstanding written communications
- Mastery of the English language
- Strong research & organization skills
- Impeccable proofreading skills
- Ability to work independently and in a team environment
- Use and provide constructive feedback to improve content quality
- Basic knowledge of digital marketing & Search Engine Optimization (SEO)
- Experience with a CMS (at least one platform, such as WordPress, Wix, Squarespace, Joomla, Drupal, etc.)
- Familiarity with major social networks (LinkedIn, Twitter, Facebook, YouTube)
- Part-time
- Flexible schedule
- Professional development assistance
- Monday to Friday
- Hybrid remote in Alexandria, VA
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3
Specialist, Medical Writing
92604 Woodbridge, California
Edwards Lifesciences
Posted 2 days ago
Job Viewed
Job Description
Patients are at the heart of everything we do. As part of our Medical Affairs team, you'll foster internal and external collaboration to generate and disseminate evidence-based clinical practices to help impact patient lives and advance the quality of care. Your scientific curiosity and passion for patients will help us grow our reach and develop innovative solutions for people fighting cardiovascular disease.
Patients with mitral and tricuspid heart valve disease often have complex conditions with limited treatment options. Our Transcatheter Mitral and Tricuspid Therapies (TMTT) business unit is boldly pursuing an innovative portfolio of technologies to address a patient's unmet clinical needs. It's our driving force to help patients live longer and healthier lives. Join us and be part of our inspiring journey.
As a key member of the Clinical Science team, the Specialist, Medical Writing is responsible for supporting the development of regulatory and clinical documents for a dynamic portfolio of products across TMTT. The Specialist should have strong scientific acumen and a commitment to putting patients first.
This position is an onsite role based at Edwards Lifesciences' corporate headquarters in Irvine, California.
**How you will make an impact:**
+ Perform and maintain systematic literature searches, contribute to the development of search terms and criteria, extract relevant clinical data, and write clear and concise summaries of the data to support the clinical evaluation and clinical study reports
+ Prepare moderately complex medical writing documents/deliverables for assigned project(s)
+ Review and provide thoughtful feedback on moderately complex cross-functional deliverables (e.g., clinical study data, risk management documents, IFUs, SSED) using clinical and technical knowledge
+ Serve as the primary contact, negotiating deliverables, timelines, and resolving project-related issues with assistance, in collaboration with cross-functional stakeholders
+ Assist in the implementation of continuous process improvements as it relates to medical writing
+ Other incidental duties
**What you'll need (required):**
+ Bachelor's Degree in a related field with 3 years of experience working in medical writing, medical affairs, clinical affairs and/or clinical science; OR
+ Master's degree in a related field with 1 year experience working in medical writing, medical affairs, clinical affairs and/or clinical science; OR
+ Doctorate degree (PhD, MD, PharmD) with relevant postdoctoral fellowship or graduate research experience.
**What else we look for (preferred):**
+ Experienced with literature reviews and various publication databases including PubMed and Embase.
+ Familiarity with the cardiovascular therapeutic area including, but not limited to, structural heart interventions, coronary interventions, heart failure, current mitral and tricuspid treatment landscape, and relevant clinical research/trials.
+ Familiarity with MEDDEV 2.7/1 and EU MDR for clinical evaluations.
+ Familiarity with FDA PMA applications.
+ Good knowledge of scientific research methodology, device development process, GCP, ICH guidelines and Global (US FDA, EU MDR) regulations.
+ Experience working in a cross functional, collaborative environment and comfortable interacting with R&D engineers, regulatory specialists, physicians, statisticians, and support personnel.
**Additional skills and general expectations:**
+ Demonstrated ability to work independently, ability to prioritize and manage multiple tasks simultaneously
+ Excellent oral and written communication skills
+ Experienced in keeping up-to-date with product developments, clinical literature, and therapeutic knowledge, and operational knowledge.
+ Advanced working knowledge with the use of MS PowerPoint, MS Word, MS Excel, EndNote, and Adobe Acrobat
+ Strong analytical, problem-solving, and scientific writing skills
+ Strict attention to detail
+ Ability to interact professionally with all organizational levels
+ Ability to work in a team environment, including inter-departmental teams and representing the organization on specific projects
+ Ability to build productive internal/external working relationships
Aligning our overall business objectives with performance, we offer competitive salaries, performance-based incentives, and a wide variety of benefits programs to address the diverse individual needs of our employees and their families.
The pay for the successful candidate will depend on various factors (e.g., qualifications, education, prior experience). Applications will be accepted while this position is posted on our Careers website.
Aligning our overall business objectives with performance, we offer competitive salaries, performance-based incentives, and a wide variety of benefits programs to address the diverse individual needs of our employees and their families.
For California (CA), the base pay range for this position is $85,000 to $120,000 (highly experienced).
The pay for the successful candidate will depend on various factors (e.g., qualifications, education, prior experience). Applications will be accepted while this position is posted on our Careers website.
Edwards is an Equal Opportunity/Affirmative Action employer including protected Veterans and individuals with disabilities.
**COVID Vaccination Requirement**
Edwards is committed to protecting our vulnerable patients and the healthcare providers who are treating them. As such, all patient-facing and in-hospital positions require COVID-19 vaccination. If hired into a covered role, as a condition of employment, you will be required to submit proof that you have been vaccinated for COVID-19, unless you request and are granted a medical or religious accommodation for exemption from the vaccination requirement. This vaccination requirement does not apply in locations where it is prohibited by law to impose vaccination.
Patients with mitral and tricuspid heart valve disease often have complex conditions with limited treatment options. Our Transcatheter Mitral and Tricuspid Therapies (TMTT) business unit is boldly pursuing an innovative portfolio of technologies to address a patient's unmet clinical needs. It's our driving force to help patients live longer and healthier lives. Join us and be part of our inspiring journey.
As a key member of the Clinical Science team, the Specialist, Medical Writing is responsible for supporting the development of regulatory and clinical documents for a dynamic portfolio of products across TMTT. The Specialist should have strong scientific acumen and a commitment to putting patients first.
This position is an onsite role based at Edwards Lifesciences' corporate headquarters in Irvine, California.
**How you will make an impact:**
+ Perform and maintain systematic literature searches, contribute to the development of search terms and criteria, extract relevant clinical data, and write clear and concise summaries of the data to support the clinical evaluation and clinical study reports
+ Prepare moderately complex medical writing documents/deliverables for assigned project(s)
+ Review and provide thoughtful feedback on moderately complex cross-functional deliverables (e.g., clinical study data, risk management documents, IFUs, SSED) using clinical and technical knowledge
+ Serve as the primary contact, negotiating deliverables, timelines, and resolving project-related issues with assistance, in collaboration with cross-functional stakeholders
+ Assist in the implementation of continuous process improvements as it relates to medical writing
+ Other incidental duties
**What you'll need (required):**
+ Bachelor's Degree in a related field with 3 years of experience working in medical writing, medical affairs, clinical affairs and/or clinical science; OR
+ Master's degree in a related field with 1 year experience working in medical writing, medical affairs, clinical affairs and/or clinical science; OR
+ Doctorate degree (PhD, MD, PharmD) with relevant postdoctoral fellowship or graduate research experience.
**What else we look for (preferred):**
+ Experienced with literature reviews and various publication databases including PubMed and Embase.
+ Familiarity with the cardiovascular therapeutic area including, but not limited to, structural heart interventions, coronary interventions, heart failure, current mitral and tricuspid treatment landscape, and relevant clinical research/trials.
+ Familiarity with MEDDEV 2.7/1 and EU MDR for clinical evaluations.
+ Familiarity with FDA PMA applications.
+ Good knowledge of scientific research methodology, device development process, GCP, ICH guidelines and Global (US FDA, EU MDR) regulations.
+ Experience working in a cross functional, collaborative environment and comfortable interacting with R&D engineers, regulatory specialists, physicians, statisticians, and support personnel.
**Additional skills and general expectations:**
+ Demonstrated ability to work independently, ability to prioritize and manage multiple tasks simultaneously
+ Excellent oral and written communication skills
+ Experienced in keeping up-to-date with product developments, clinical literature, and therapeutic knowledge, and operational knowledge.
+ Advanced working knowledge with the use of MS PowerPoint, MS Word, MS Excel, EndNote, and Adobe Acrobat
+ Strong analytical, problem-solving, and scientific writing skills
+ Strict attention to detail
+ Ability to interact professionally with all organizational levels
+ Ability to work in a team environment, including inter-departmental teams and representing the organization on specific projects
+ Ability to build productive internal/external working relationships
Aligning our overall business objectives with performance, we offer competitive salaries, performance-based incentives, and a wide variety of benefits programs to address the diverse individual needs of our employees and their families.
The pay for the successful candidate will depend on various factors (e.g., qualifications, education, prior experience). Applications will be accepted while this position is posted on our Careers website.
Aligning our overall business objectives with performance, we offer competitive salaries, performance-based incentives, and a wide variety of benefits programs to address the diverse individual needs of our employees and their families.
For California (CA), the base pay range for this position is $85,000 to $120,000 (highly experienced).
The pay for the successful candidate will depend on various factors (e.g., qualifications, education, prior experience). Applications will be accepted while this position is posted on our Careers website.
Edwards is an Equal Opportunity/Affirmative Action employer including protected Veterans and individuals with disabilities.
**COVID Vaccination Requirement**
Edwards is committed to protecting our vulnerable patients and the healthcare providers who are treating them. As such, all patient-facing and in-hospital positions require COVID-19 vaccination. If hired into a covered role, as a condition of employment, you will be required to submit proof that you have been vaccinated for COVID-19, unless you request and are granted a medical or religious accommodation for exemption from the vaccination requirement. This vaccination requirement does not apply in locations where it is prohibited by law to impose vaccination.
View Now
4
Specialist, Medical Writing
90006 Los Angeles, California
Edwards Lifesciences
Posted 2 days ago
Job Viewed
Job Description
Patients are at the heart of everything we do. As part of our Medical Affairs team, you'll foster internal and external collaboration to generate and disseminate evidence-based clinical practices to help impact patient lives and advance the quality of care. Your scientific curiosity and passion for patients will help us grow our reach and develop innovative solutions for people fighting cardiovascular disease.
Patients with mitral and tricuspid heart valve disease often have complex conditions with limited treatment options. Our Transcatheter Mitral and Tricuspid Therapies (TMTT) business unit is boldly pursuing an innovative portfolio of technologies to address a patient's unmet clinical needs. It's our driving force to help patients live longer and healthier lives. Join us and be part of our inspiring journey.
As a key member of the Clinical Science team, the Specialist, Medical Writing is responsible for supporting the development of regulatory and clinical documents for a dynamic portfolio of products across TMTT. The Specialist should have strong scientific acumen and a commitment to putting patients first.
This position is an onsite role based at Edwards Lifesciences' corporate headquarters in Irvine, California.
**How you will make an impact:**
+ Perform and maintain systematic literature searches, contribute to the development of search terms and criteria, extract relevant clinical data, and write clear and concise summaries of the data to support the clinical evaluation and clinical study reports
+ Prepare moderately complex medical writing documents/deliverables for assigned project(s)
+ Review and provide thoughtful feedback on moderately complex cross-functional deliverables (e.g., clinical study data, risk management documents, IFUs, SSED) using clinical and technical knowledge
+ Serve as the primary contact, negotiating deliverables, timelines, and resolving project-related issues with assistance, in collaboration with cross-functional stakeholders
+ Assist in the implementation of continuous process improvements as it relates to medical writing
+ Other incidental duties
**What you'll need (required):**
+ Bachelor's Degree in a related field with 3 years of experience working in medical writing, medical affairs, clinical affairs and/or clinical science; OR
+ Master's degree in a related field with 1 year experience working in medical writing, medical affairs, clinical affairs and/or clinical science; OR
+ Doctorate degree (PhD, MD, PharmD) with relevant postdoctoral fellowship or graduate research experience.
**What else we look for (preferred):**
+ Experienced with literature reviews and various publication databases including PubMed and Embase.
+ Familiarity with the cardiovascular therapeutic area including, but not limited to, structural heart interventions, coronary interventions, heart failure, current mitral and tricuspid treatment landscape, and relevant clinical research/trials.
+ Familiarity with MEDDEV 2.7/1 and EU MDR for clinical evaluations.
+ Familiarity with FDA PMA applications.
+ Good knowledge of scientific research methodology, device development process, GCP, ICH guidelines and Global (US FDA, EU MDR) regulations.
+ Experience working in a cross functional, collaborative environment and comfortable interacting with R&D engineers, regulatory specialists, physicians, statisticians, and support personnel.
**Additional skills and general expectations:**
+ Demonstrated ability to work independently, ability to prioritize and manage multiple tasks simultaneously
+ Excellent oral and written communication skills
+ Experienced in keeping up-to-date with product developments, clinical literature, and therapeutic knowledge, and operational knowledge.
+ Advanced working knowledge with the use of MS PowerPoint, MS Word, MS Excel, EndNote, and Adobe Acrobat
+ Strong analytical, problem-solving, and scientific writing skills
+ Strict attention to detail
+ Ability to interact professionally with all organizational levels
+ Ability to work in a team environment, including inter-departmental teams and representing the organization on specific projects
+ Ability to build productive internal/external working relationships
Aligning our overall business objectives with performance, we offer competitive salaries, performance-based incentives, and a wide variety of benefits programs to address the diverse individual needs of our employees and their families.
The pay for the successful candidate will depend on various factors (e.g., qualifications, education, prior experience). Applications will be accepted while this position is posted on our Careers website.
Aligning our overall business objectives with performance, we offer competitive salaries, performance-based incentives, and a wide variety of benefits programs to address the diverse individual needs of our employees and their families.
For California (CA), the base pay range for this position is $85,000 to $120,000 (highly experienced).
The pay for the successful candidate will depend on various factors (e.g., qualifications, education, prior experience). Applications will be accepted while this position is posted on our Careers website.
Edwards is an Equal Opportunity/Affirmative Action employer including protected Veterans and individuals with disabilities.
**COVID Vaccination Requirement**
Edwards is committed to protecting our vulnerable patients and the healthcare providers who are treating them. As such, all patient-facing and in-hospital positions require COVID-19 vaccination. If hired into a covered role, as a condition of employment, you will be required to submit proof that you have been vaccinated for COVID-19, unless you request and are granted a medical or religious accommodation for exemption from the vaccination requirement. This vaccination requirement does not apply in locations where it is prohibited by law to impose vaccination.
Patients with mitral and tricuspid heart valve disease often have complex conditions with limited treatment options. Our Transcatheter Mitral and Tricuspid Therapies (TMTT) business unit is boldly pursuing an innovative portfolio of technologies to address a patient's unmet clinical needs. It's our driving force to help patients live longer and healthier lives. Join us and be part of our inspiring journey.
As a key member of the Clinical Science team, the Specialist, Medical Writing is responsible for supporting the development of regulatory and clinical documents for a dynamic portfolio of products across TMTT. The Specialist should have strong scientific acumen and a commitment to putting patients first.
This position is an onsite role based at Edwards Lifesciences' corporate headquarters in Irvine, California.
**How you will make an impact:**
+ Perform and maintain systematic literature searches, contribute to the development of search terms and criteria, extract relevant clinical data, and write clear and concise summaries of the data to support the clinical evaluation and clinical study reports
+ Prepare moderately complex medical writing documents/deliverables for assigned project(s)
+ Review and provide thoughtful feedback on moderately complex cross-functional deliverables (e.g., clinical study data, risk management documents, IFUs, SSED) using clinical and technical knowledge
+ Serve as the primary contact, negotiating deliverables, timelines, and resolving project-related issues with assistance, in collaboration with cross-functional stakeholders
+ Assist in the implementation of continuous process improvements as it relates to medical writing
+ Other incidental duties
**What you'll need (required):**
+ Bachelor's Degree in a related field with 3 years of experience working in medical writing, medical affairs, clinical affairs and/or clinical science; OR
+ Master's degree in a related field with 1 year experience working in medical writing, medical affairs, clinical affairs and/or clinical science; OR
+ Doctorate degree (PhD, MD, PharmD) with relevant postdoctoral fellowship or graduate research experience.
**What else we look for (preferred):**
+ Experienced with literature reviews and various publication databases including PubMed and Embase.
+ Familiarity with the cardiovascular therapeutic area including, but not limited to, structural heart interventions, coronary interventions, heart failure, current mitral and tricuspid treatment landscape, and relevant clinical research/trials.
+ Familiarity with MEDDEV 2.7/1 and EU MDR for clinical evaluations.
+ Familiarity with FDA PMA applications.
+ Good knowledge of scientific research methodology, device development process, GCP, ICH guidelines and Global (US FDA, EU MDR) regulations.
+ Experience working in a cross functional, collaborative environment and comfortable interacting with R&D engineers, regulatory specialists, physicians, statisticians, and support personnel.
**Additional skills and general expectations:**
+ Demonstrated ability to work independently, ability to prioritize and manage multiple tasks simultaneously
+ Excellent oral and written communication skills
+ Experienced in keeping up-to-date with product developments, clinical literature, and therapeutic knowledge, and operational knowledge.
+ Advanced working knowledge with the use of MS PowerPoint, MS Word, MS Excel, EndNote, and Adobe Acrobat
+ Strong analytical, problem-solving, and scientific writing skills
+ Strict attention to detail
+ Ability to interact professionally with all organizational levels
+ Ability to work in a team environment, including inter-departmental teams and representing the organization on specific projects
+ Ability to build productive internal/external working relationships
Aligning our overall business objectives with performance, we offer competitive salaries, performance-based incentives, and a wide variety of benefits programs to address the diverse individual needs of our employees and their families.
The pay for the successful candidate will depend on various factors (e.g., qualifications, education, prior experience). Applications will be accepted while this position is posted on our Careers website.
Aligning our overall business objectives with performance, we offer competitive salaries, performance-based incentives, and a wide variety of benefits programs to address the diverse individual needs of our employees and their families.
For California (CA), the base pay range for this position is $85,000 to $120,000 (highly experienced).
The pay for the successful candidate will depend on various factors (e.g., qualifications, education, prior experience). Applications will be accepted while this position is posted on our Careers website.
Edwards is an Equal Opportunity/Affirmative Action employer including protected Veterans and individuals with disabilities.
**COVID Vaccination Requirement**
Edwards is committed to protecting our vulnerable patients and the healthcare providers who are treating them. As such, all patient-facing and in-hospital positions require COVID-19 vaccination. If hired into a covered role, as a condition of employment, you will be required to submit proof that you have been vaccinated for COVID-19, unless you request and are granted a medical or religious accommodation for exemption from the vaccination requirement. This vaccination requirement does not apply in locations where it is prohibited by law to impose vaccination.
View Now
5
Specialist, Medical Writing
92108 Mission Valley, California
Edwards Lifesciences
Posted 2 days ago
Job Viewed
Job Description
Patients are at the heart of everything we do. As part of our Medical Affairs team, you'll foster internal and external collaboration to generate and disseminate evidence-based clinical practices to help impact patient lives and advance the quality of care. Your scientific curiosity and passion for patients will help us grow our reach and develop innovative solutions for people fighting cardiovascular disease.
Patients with mitral and tricuspid heart valve disease often have complex conditions with limited treatment options. Our Transcatheter Mitral and Tricuspid Therapies (TMTT) business unit is boldly pursuing an innovative portfolio of technologies to address a patient's unmet clinical needs. It's our driving force to help patients live longer and healthier lives. Join us and be part of our inspiring journey.
As a key member of the Clinical Science team, the Specialist, Medical Writing is responsible for supporting the development of regulatory and clinical documents for a dynamic portfolio of products across TMTT. The Specialist should have strong scientific acumen and a commitment to putting patients first.
This position is an onsite role based at Edwards Lifesciences' corporate headquarters in Irvine, California.
**How you will make an impact:**
+ Perform and maintain systematic literature searches, contribute to the development of search terms and criteria, extract relevant clinical data, and write clear and concise summaries of the data to support the clinical evaluation and clinical study reports
+ Prepare moderately complex medical writing documents/deliverables for assigned project(s)
+ Review and provide thoughtful feedback on moderately complex cross-functional deliverables (e.g., clinical study data, risk management documents, IFUs, SSED) using clinical and technical knowledge
+ Serve as the primary contact, negotiating deliverables, timelines, and resolving project-related issues with assistance, in collaboration with cross-functional stakeholders
+ Assist in the implementation of continuous process improvements as it relates to medical writing
+ Other incidental duties
**What you'll need (required):**
+ Bachelor's Degree in a related field with 3 years of experience working in medical writing, medical affairs, clinical affairs and/or clinical science; OR
+ Master's degree in a related field with 1 year experience working in medical writing, medical affairs, clinical affairs and/or clinical science; OR
+ Doctorate degree (PhD, MD, PharmD) with relevant postdoctoral fellowship or graduate research experience.
**What else we look for (preferred):**
+ Experienced with literature reviews and various publication databases including PubMed and Embase.
+ Familiarity with the cardiovascular therapeutic area including, but not limited to, structural heart interventions, coronary interventions, heart failure, current mitral and tricuspid treatment landscape, and relevant clinical research/trials.
+ Familiarity with MEDDEV 2.7/1 and EU MDR for clinical evaluations.
+ Familiarity with FDA PMA applications.
+ Good knowledge of scientific research methodology, device development process, GCP, ICH guidelines and Global (US FDA, EU MDR) regulations.
+ Experience working in a cross functional, collaborative environment and comfortable interacting with R&D engineers, regulatory specialists, physicians, statisticians, and support personnel.
**Additional skills and general expectations:**
+ Demonstrated ability to work independently, ability to prioritize and manage multiple tasks simultaneously
+ Excellent oral and written communication skills
+ Experienced in keeping up-to-date with product developments, clinical literature, and therapeutic knowledge, and operational knowledge.
+ Advanced working knowledge with the use of MS PowerPoint, MS Word, MS Excel, EndNote, and Adobe Acrobat
+ Strong analytical, problem-solving, and scientific writing skills
+ Strict attention to detail
+ Ability to interact professionally with all organizational levels
+ Ability to work in a team environment, including inter-departmental teams and representing the organization on specific projects
+ Ability to build productive internal/external working relationships
Aligning our overall business objectives with performance, we offer competitive salaries, performance-based incentives, and a wide variety of benefits programs to address the diverse individual needs of our employees and their families.
The pay for the successful candidate will depend on various factors (e.g., qualifications, education, prior experience). Applications will be accepted while this position is posted on our Careers website.
Aligning our overall business objectives with performance, we offer competitive salaries, performance-based incentives, and a wide variety of benefits programs to address the diverse individual needs of our employees and their families.
For California (CA), the base pay range for this position is $85,000 to $120,000 (highly experienced).
The pay for the successful candidate will depend on various factors (e.g., qualifications, education, prior experience). Applications will be accepted while this position is posted on our Careers website.
Edwards is an Equal Opportunity/Affirmative Action employer including protected Veterans and individuals with disabilities.
**COVID Vaccination Requirement**
Edwards is committed to protecting our vulnerable patients and the healthcare providers who are treating them. As such, all patient-facing and in-hospital positions require COVID-19 vaccination. If hired into a covered role, as a condition of employment, you will be required to submit proof that you have been vaccinated for COVID-19, unless you request and are granted a medical or religious accommodation for exemption from the vaccination requirement. This vaccination requirement does not apply in locations where it is prohibited by law to impose vaccination.
Patients with mitral and tricuspid heart valve disease often have complex conditions with limited treatment options. Our Transcatheter Mitral and Tricuspid Therapies (TMTT) business unit is boldly pursuing an innovative portfolio of technologies to address a patient's unmet clinical needs. It's our driving force to help patients live longer and healthier lives. Join us and be part of our inspiring journey.
As a key member of the Clinical Science team, the Specialist, Medical Writing is responsible for supporting the development of regulatory and clinical documents for a dynamic portfolio of products across TMTT. The Specialist should have strong scientific acumen and a commitment to putting patients first.
This position is an onsite role based at Edwards Lifesciences' corporate headquarters in Irvine, California.
**How you will make an impact:**
+ Perform and maintain systematic literature searches, contribute to the development of search terms and criteria, extract relevant clinical data, and write clear and concise summaries of the data to support the clinical evaluation and clinical study reports
+ Prepare moderately complex medical writing documents/deliverables for assigned project(s)
+ Review and provide thoughtful feedback on moderately complex cross-functional deliverables (e.g., clinical study data, risk management documents, IFUs, SSED) using clinical and technical knowledge
+ Serve as the primary contact, negotiating deliverables, timelines, and resolving project-related issues with assistance, in collaboration with cross-functional stakeholders
+ Assist in the implementation of continuous process improvements as it relates to medical writing
+ Other incidental duties
**What you'll need (required):**
+ Bachelor's Degree in a related field with 3 years of experience working in medical writing, medical affairs, clinical affairs and/or clinical science; OR
+ Master's degree in a related field with 1 year experience working in medical writing, medical affairs, clinical affairs and/or clinical science; OR
+ Doctorate degree (PhD, MD, PharmD) with relevant postdoctoral fellowship or graduate research experience.
**What else we look for (preferred):**
+ Experienced with literature reviews and various publication databases including PubMed and Embase.
+ Familiarity with the cardiovascular therapeutic area including, but not limited to, structural heart interventions, coronary interventions, heart failure, current mitral and tricuspid treatment landscape, and relevant clinical research/trials.
+ Familiarity with MEDDEV 2.7/1 and EU MDR for clinical evaluations.
+ Familiarity with FDA PMA applications.
+ Good knowledge of scientific research methodology, device development process, GCP, ICH guidelines and Global (US FDA, EU MDR) regulations.
+ Experience working in a cross functional, collaborative environment and comfortable interacting with R&D engineers, regulatory specialists, physicians, statisticians, and support personnel.
**Additional skills and general expectations:**
+ Demonstrated ability to work independently, ability to prioritize and manage multiple tasks simultaneously
+ Excellent oral and written communication skills
+ Experienced in keeping up-to-date with product developments, clinical literature, and therapeutic knowledge, and operational knowledge.
+ Advanced working knowledge with the use of MS PowerPoint, MS Word, MS Excel, EndNote, and Adobe Acrobat
+ Strong analytical, problem-solving, and scientific writing skills
+ Strict attention to detail
+ Ability to interact professionally with all organizational levels
+ Ability to work in a team environment, including inter-departmental teams and representing the organization on specific projects
+ Ability to build productive internal/external working relationships
Aligning our overall business objectives with performance, we offer competitive salaries, performance-based incentives, and a wide variety of benefits programs to address the diverse individual needs of our employees and their families.
The pay for the successful candidate will depend on various factors (e.g., qualifications, education, prior experience). Applications will be accepted while this position is posted on our Careers website.
Aligning our overall business objectives with performance, we offer competitive salaries, performance-based incentives, and a wide variety of benefits programs to address the diverse individual needs of our employees and their families.
For California (CA), the base pay range for this position is $85,000 to $120,000 (highly experienced).
The pay for the successful candidate will depend on various factors (e.g., qualifications, education, prior experience). Applications will be accepted while this position is posted on our Careers website.
Edwards is an Equal Opportunity/Affirmative Action employer including protected Veterans and individuals with disabilities.
**COVID Vaccination Requirement**
Edwards is committed to protecting our vulnerable patients and the healthcare providers who are treating them. As such, all patient-facing and in-hospital positions require COVID-19 vaccination. If hired into a covered role, as a condition of employment, you will be required to submit proof that you have been vaccinated for COVID-19, unless you request and are granted a medical or religious accommodation for exemption from the vaccination requirement. This vaccination requirement does not apply in locations where it is prohibited by law to impose vaccination.
View Now
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6
Specialist, Medical Writing
92516 Riverside, California
Edwards Lifesciences
Posted 2 days ago
Job Viewed
Job Description
Patients are at the heart of everything we do. As part of our Medical Affairs team, you'll foster internal and external collaboration to generate and disseminate evidence-based clinical practices to help impact patient lives and advance the quality of care. Your scientific curiosity and passion for patients will help us grow our reach and develop innovative solutions for people fighting cardiovascular disease.
Patients with mitral and tricuspid heart valve disease often have complex conditions with limited treatment options. Our Transcatheter Mitral and Tricuspid Therapies (TMTT) business unit is boldly pursuing an innovative portfolio of technologies to address a patient's unmet clinical needs. It's our driving force to help patients live longer and healthier lives. Join us and be part of our inspiring journey.
As a key member of the Clinical Science team, the Specialist, Medical Writing is responsible for supporting the development of regulatory and clinical documents for a dynamic portfolio of products across TMTT. The Specialist should have strong scientific acumen and a commitment to putting patients first.
This position is an onsite role based at Edwards Lifesciences' corporate headquarters in Irvine, California.
**How you will make an impact:**
+ Perform and maintain systematic literature searches, contribute to the development of search terms and criteria, extract relevant clinical data, and write clear and concise summaries of the data to support the clinical evaluation and clinical study reports
+ Prepare moderately complex medical writing documents/deliverables for assigned project(s)
+ Review and provide thoughtful feedback on moderately complex cross-functional deliverables (e.g., clinical study data, risk management documents, IFUs, SSED) using clinical and technical knowledge
+ Serve as the primary contact, negotiating deliverables, timelines, and resolving project-related issues with assistance, in collaboration with cross-functional stakeholders
+ Assist in the implementation of continuous process improvements as it relates to medical writing
+ Other incidental duties
**What you'll need (required):**
+ Bachelor's Degree in a related field with 3 years of experience working in medical writing, medical affairs, clinical affairs and/or clinical science; OR
+ Master's degree in a related field with 1 year experience working in medical writing, medical affairs, clinical affairs and/or clinical science; OR
+ Doctorate degree (PhD, MD, PharmD) with relevant postdoctoral fellowship or graduate research experience.
**What else we look for (preferred):**
+ Experienced with literature reviews and various publication databases including PubMed and Embase.
+ Familiarity with the cardiovascular therapeutic area including, but not limited to, structural heart interventions, coronary interventions, heart failure, current mitral and tricuspid treatment landscape, and relevant clinical research/trials.
+ Familiarity with MEDDEV 2.7/1 and EU MDR for clinical evaluations.
+ Familiarity with FDA PMA applications.
+ Good knowledge of scientific research methodology, device development process, GCP, ICH guidelines and Global (US FDA, EU MDR) regulations.
+ Experience working in a cross functional, collaborative environment and comfortable interacting with R&D engineers, regulatory specialists, physicians, statisticians, and support personnel.
**Additional skills and general expectations:**
+ Demonstrated ability to work independently, ability to prioritize and manage multiple tasks simultaneously
+ Excellent oral and written communication skills
+ Experienced in keeping up-to-date with product developments, clinical literature, and therapeutic knowledge, and operational knowledge.
+ Advanced working knowledge with the use of MS PowerPoint, MS Word, MS Excel, EndNote, and Adobe Acrobat
+ Strong analytical, problem-solving, and scientific writing skills
+ Strict attention to detail
+ Ability to interact professionally with all organizational levels
+ Ability to work in a team environment, including inter-departmental teams and representing the organization on specific projects
+ Ability to build productive internal/external working relationships
Aligning our overall business objectives with performance, we offer competitive salaries, performance-based incentives, and a wide variety of benefits programs to address the diverse individual needs of our employees and their families.
The pay for the successful candidate will depend on various factors (e.g., qualifications, education, prior experience). Applications will be accepted while this position is posted on our Careers website.
Aligning our overall business objectives with performance, we offer competitive salaries, performance-based incentives, and a wide variety of benefits programs to address the diverse individual needs of our employees and their families.
For California (CA), the base pay range for this position is $85,000 to $120,000 (highly experienced).
The pay for the successful candidate will depend on various factors (e.g., qualifications, education, prior experience). Applications will be accepted while this position is posted on our Careers website.
Edwards is an Equal Opportunity/Affirmative Action employer including protected Veterans and individuals with disabilities.
**COVID Vaccination Requirement**
Edwards is committed to protecting our vulnerable patients and the healthcare providers who are treating them. As such, all patient-facing and in-hospital positions require COVID-19 vaccination. If hired into a covered role, as a condition of employment, you will be required to submit proof that you have been vaccinated for COVID-19, unless you request and are granted a medical or religious accommodation for exemption from the vaccination requirement. This vaccination requirement does not apply in locations where it is prohibited by law to impose vaccination.
Patients with mitral and tricuspid heart valve disease often have complex conditions with limited treatment options. Our Transcatheter Mitral and Tricuspid Therapies (TMTT) business unit is boldly pursuing an innovative portfolio of technologies to address a patient's unmet clinical needs. It's our driving force to help patients live longer and healthier lives. Join us and be part of our inspiring journey.
As a key member of the Clinical Science team, the Specialist, Medical Writing is responsible for supporting the development of regulatory and clinical documents for a dynamic portfolio of products across TMTT. The Specialist should have strong scientific acumen and a commitment to putting patients first.
This position is an onsite role based at Edwards Lifesciences' corporate headquarters in Irvine, California.
**How you will make an impact:**
+ Perform and maintain systematic literature searches, contribute to the development of search terms and criteria, extract relevant clinical data, and write clear and concise summaries of the data to support the clinical evaluation and clinical study reports
+ Prepare moderately complex medical writing documents/deliverables for assigned project(s)
+ Review and provide thoughtful feedback on moderately complex cross-functional deliverables (e.g., clinical study data, risk management documents, IFUs, SSED) using clinical and technical knowledge
+ Serve as the primary contact, negotiating deliverables, timelines, and resolving project-related issues with assistance, in collaboration with cross-functional stakeholders
+ Assist in the implementation of continuous process improvements as it relates to medical writing
+ Other incidental duties
**What you'll need (required):**
+ Bachelor's Degree in a related field with 3 years of experience working in medical writing, medical affairs, clinical affairs and/or clinical science; OR
+ Master's degree in a related field with 1 year experience working in medical writing, medical affairs, clinical affairs and/or clinical science; OR
+ Doctorate degree (PhD, MD, PharmD) with relevant postdoctoral fellowship or graduate research experience.
**What else we look for (preferred):**
+ Experienced with literature reviews and various publication databases including PubMed and Embase.
+ Familiarity with the cardiovascular therapeutic area including, but not limited to, structural heart interventions, coronary interventions, heart failure, current mitral and tricuspid treatment landscape, and relevant clinical research/trials.
+ Familiarity with MEDDEV 2.7/1 and EU MDR for clinical evaluations.
+ Familiarity with FDA PMA applications.
+ Good knowledge of scientific research methodology, device development process, GCP, ICH guidelines and Global (US FDA, EU MDR) regulations.
+ Experience working in a cross functional, collaborative environment and comfortable interacting with R&D engineers, regulatory specialists, physicians, statisticians, and support personnel.
**Additional skills and general expectations:**
+ Demonstrated ability to work independently, ability to prioritize and manage multiple tasks simultaneously
+ Excellent oral and written communication skills
+ Experienced in keeping up-to-date with product developments, clinical literature, and therapeutic knowledge, and operational knowledge.
+ Advanced working knowledge with the use of MS PowerPoint, MS Word, MS Excel, EndNote, and Adobe Acrobat
+ Strong analytical, problem-solving, and scientific writing skills
+ Strict attention to detail
+ Ability to interact professionally with all organizational levels
+ Ability to work in a team environment, including inter-departmental teams and representing the organization on specific projects
+ Ability to build productive internal/external working relationships
Aligning our overall business objectives with performance, we offer competitive salaries, performance-based incentives, and a wide variety of benefits programs to address the diverse individual needs of our employees and their families.
The pay for the successful candidate will depend on various factors (e.g., qualifications, education, prior experience). Applications will be accepted while this position is posted on our Careers website.
Aligning our overall business objectives with performance, we offer competitive salaries, performance-based incentives, and a wide variety of benefits programs to address the diverse individual needs of our employees and their families.
For California (CA), the base pay range for this position is $85,000 to $120,000 (highly experienced).
The pay for the successful candidate will depend on various factors (e.g., qualifications, education, prior experience). Applications will be accepted while this position is posted on our Careers website.
Edwards is an Equal Opportunity/Affirmative Action employer including protected Veterans and individuals with disabilities.
**COVID Vaccination Requirement**
Edwards is committed to protecting our vulnerable patients and the healthcare providers who are treating them. As such, all patient-facing and in-hospital positions require COVID-19 vaccination. If hired into a covered role, as a condition of employment, you will be required to submit proof that you have been vaccinated for COVID-19, unless you request and are granted a medical or religious accommodation for exemption from the vaccination requirement. This vaccination requirement does not apply in locations where it is prohibited by law to impose vaccination.
View Now
7
Writing Center Assistant
60439 Lemont, Illinois
Argonne National Laboratory
Posted 5 days ago
Job Viewed
Job Description
The Writing Center of Excellence in the Communication and Public Affairs Division at Argonne National Laboratory seeks a Writing Center Assistant to support a variety of Writing Center communication and support functions. In this role, you will create, revise, and format documents, forms, and policies, as well as edit and upload media, events, and policy files to the web. You will proofread documents to ensure accuracy and compliance with accessibility standards (508 compliance) and style guides, and assist with formatting and troubleshooting document issues.
In addition to communication-related tasks, you will provide administrative support to ensure the smooth operation of the Writing Center. Responsibilities include project tracking and reporting, assisting with onboarding new staff and contractors, and handling customer requests for Writing Center support. You will also help ensure accurate records on customer projects and time reporting by staff and contractors. This position requires someone who can work independently with minimal supervision while collaborating effectively with team members and customers. The ideal candidate is detail oriented, organized, and able to balance multiple responsibilities in a fast-paced environment.
A world-leading science laboratory, Argonne's research portfolio spans the spectrum from fundamental to applied sciences. Laboratory researchers pursue big, ambitious ideas with international impact in areas as diverse as biology, quantum information science, new materials, and artificial intelligence. Argonne operates large research facilities that serve more than 7,000 researchers from around the world each year, and partners with academic, government, industrial, and community organizations to drive pivotal discoveries and foster groundbreaking innovations.
**Position Requirements**
+ Expertise in various software programs, including Word, Adobe Acrobat Pro, and Excel.
+ Experience in tracking and reporting project metrics.
+ Experience in posting content to the web.
+ Knowledge of AI tools to increase efficiency and effectiveness a plus.
+ Excellent planning and organizational skills, plus attention to detail.
+ Ability to prioritize, plan, track, and deliver projects and services on time in a fast-paced environment, while remaining flexible.
+ Ability to lightly edit and proofread documents.
+ Experience in writing and editing in alignment with a style guide, such as the University of Chicago Style Guide and Associated Press Stylebook.
+ Strong customer-service focus.
+ Steward of lab resources.
+ Passion for the mission of the lab.
+ Ability to model Argonne's Core Values: Impact, Safety, Respect, Integrity, and Teamwork.
+ Associates Degree with 8+ years of experience, graphic communications/design, journalism, or a related communications field.
**Job Family**
Support Administrative (SA)
**Job Profile**
Administrative Support 4
**Worker Type**
Regular
**Time Type**
Full time
The expected hiring range for this position is $30.17 - $45.13.
Please note that the pay range information is a general guideline only. The pay offered to a selected candidate will be determined based on factors such as, but not limited to, the scope and responsibilities of the position, the qualifications of the selected candidate, business considerations, internal equity, and external market pay for comparable jobs. Additionally, comprehensive benefits are part of the total rewards package.
Click here ( to view Argonne employee benefits!
_As an equal employment opportunity employer, and in accordance with our core values of impact, safety, respect, integrity and teamwork, Argonne National Laboratory is committed to a safe and welcoming workplace that fosters collaborative scientific discovery and innovation. Argonne encourages everyone to apply for employment. Argonne is committed to nondiscrimination and considers all qualified applicants for employment without regard to any characteristic protected by law._
_Argonne employees, and certain guest researchers and contractors, are subject to particular restrictions related to participation in Foreign Government Sponsored or Affiliated Activities, as defined and detailed in United States Department of Energy Order 486.1A. You will be asked to disclose any such participation in the application phase for review by Argonne's Legal Department._
_All Argonne offers of employment are contingent upon a background check that includes an assessment of criminal conviction history conducted on an individualized and case-by-case basis. Please be advised that Argonne positions require upon hire (or may require in the future) for the individual be to obtain a government access authorization that involves additional background check requirements. Failure to obtain or maintain such government access authorization could result in the withdrawal of a job offer or future termination of employment._
In addition to communication-related tasks, you will provide administrative support to ensure the smooth operation of the Writing Center. Responsibilities include project tracking and reporting, assisting with onboarding new staff and contractors, and handling customer requests for Writing Center support. You will also help ensure accurate records on customer projects and time reporting by staff and contractors. This position requires someone who can work independently with minimal supervision while collaborating effectively with team members and customers. The ideal candidate is detail oriented, organized, and able to balance multiple responsibilities in a fast-paced environment.
A world-leading science laboratory, Argonne's research portfolio spans the spectrum from fundamental to applied sciences. Laboratory researchers pursue big, ambitious ideas with international impact in areas as diverse as biology, quantum information science, new materials, and artificial intelligence. Argonne operates large research facilities that serve more than 7,000 researchers from around the world each year, and partners with academic, government, industrial, and community organizations to drive pivotal discoveries and foster groundbreaking innovations.
**Position Requirements**
+ Expertise in various software programs, including Word, Adobe Acrobat Pro, and Excel.
+ Experience in tracking and reporting project metrics.
+ Experience in posting content to the web.
+ Knowledge of AI tools to increase efficiency and effectiveness a plus.
+ Excellent planning and organizational skills, plus attention to detail.
+ Ability to prioritize, plan, track, and deliver projects and services on time in a fast-paced environment, while remaining flexible.
+ Ability to lightly edit and proofread documents.
+ Experience in writing and editing in alignment with a style guide, such as the University of Chicago Style Guide and Associated Press Stylebook.
+ Strong customer-service focus.
+ Steward of lab resources.
+ Passion for the mission of the lab.
+ Ability to model Argonne's Core Values: Impact, Safety, Respect, Integrity, and Teamwork.
+ Associates Degree with 8+ years of experience, graphic communications/design, journalism, or a related communications field.
**Job Family**
Support Administrative (SA)
**Job Profile**
Administrative Support 4
**Worker Type**
Regular
**Time Type**
Full time
The expected hiring range for this position is $30.17 - $45.13.
Please note that the pay range information is a general guideline only. The pay offered to a selected candidate will be determined based on factors such as, but not limited to, the scope and responsibilities of the position, the qualifications of the selected candidate, business considerations, internal equity, and external market pay for comparable jobs. Additionally, comprehensive benefits are part of the total rewards package.
Click here ( to view Argonne employee benefits!
_As an equal employment opportunity employer, and in accordance with our core values of impact, safety, respect, integrity and teamwork, Argonne National Laboratory is committed to a safe and welcoming workplace that fosters collaborative scientific discovery and innovation. Argonne encourages everyone to apply for employment. Argonne is committed to nondiscrimination and considers all qualified applicants for employment without regard to any characteristic protected by law._
_Argonne employees, and certain guest researchers and contractors, are subject to particular restrictions related to participation in Foreign Government Sponsored or Affiliated Activities, as defined and detailed in United States Department of Energy Order 486.1A. You will be asked to disclose any such participation in the application phase for review by Argonne's Legal Department._
_All Argonne offers of employment are contingent upon a background check that includes an assessment of criminal conviction history conducted on an individualized and case-by-case basis. Please be advised that Argonne positions require upon hire (or may require in the future) for the individual be to obtain a government access authorization that involves additional background check requirements. Failure to obtain or maintain such government access authorization could result in the withdrawal of a job offer or future termination of employment._
View Now
8
Technical Writing Intern
02133 Boston, Kentucky
Red Hat
Posted 7 days ago
Job Viewed
Job Description
**Job Summary:**
We are currently looking for Technical Writing interns to join us in Boston, MA or Raleigh, NC. You will work closely with a senior mentor to gain technical knowledge and experience in your field, and cooperate with a broader international team both locally and globally. As a Technical Writer, you'll assist in the creation of feature documentation, user guides, and premium content that accompany our solutions. You will also work on effective scoping, quality testing, and delivery of writing projects, maintain a customer focus by participating in existing programs, and grow your technical expertise and strength.
In this role, you will work in an environment where different perspectives are invited, the best ideas are valued, and people feel empowered to contribute. Freedom and courage are two of our core values, which is why you can practice taking risks and exploring the unknown and developing strengths. Yet being a Red Hatter isn't just about being brave; it's also about demonstrating commitment and sticking to it.
The focus for Red Hat's Intern Program is a dual partnership between the Emerging Talent Team, and our intern managers. We can offer you professional development, social engagement and networking, performance and development, and meaningful work throughout your time at Red Hat.
**Job Responsibilities:**
+ Work closely with content strategists, engineering project teams, technical writers, and other stakeholders to produce and maintain high-quality documentation for upcoming Red Hat solution releases.
+ Engage and collaborate with the closed-loop customer feedback program to address content gaps, act on direct customer feedback, and promote continuous improvement on the documentation experience.
+ Effectively manage documentation projects and deliver customer-focused documentation
+ Gain expertise in the use of our internal documentation toolchain, including the publishing platform and issue tracking tools
+ Network with other talented interns in an inclusive workplace where you can be yourself and thrive
**Required Skills:**
+ Excellent written and verbal communication skills in English
+ Ability to read, write, and compile technical documents, including feature descriptions, customer use cases, and release notes
+ Ability to effectively establish and maintain communication with subject matter experts and other project team members.
+ Passion, curiosity, and desire to create new things and examine how things work internally
+ Willingness to learn and proactivity work as a part of a wider team
**About Red Hat**
Red Hat ( is the world's leading provider of enterprise open source ( software solutions, using a community-powered approach to deliver high-performing Linux, cloud, container, and Kubernetes technologies. Spread across 40+ countries, our associates work flexibly across work environments, from in-office, to office-flex, to fully remote, depending on the requirements of their role. Red Hatters are encouraged to bring their best ideas, no matter their title or tenure. We're a leader in open source because of our open and inclusive environment. We hire creative, passionate people ready to contribute their ideas, help solve complex problems, and make an impact.
**Inclusion at Red Hat**
Red Hat's culture is built on the open source principles of transparency, collaboration, and inclusion, where the best ideas can come from anywhere and anyone. When this is realized, it empowers people from different backgrounds, perspectives, and experiences to come together to share ideas, challenge the status quo, and drive innovation. Our aspiration is that everyone experiences this culture with equal opportunity and access, and that all voices are not only heard but also celebrated. We hope you will join our celebration, and we welcome and encourage applicants from all the beautiful dimensions that compose our global village.
**Equal Opportunity Policy (EEO)**
Red Hat is proud to be an equal opportunity workplace and an affirmative action employer. We review applications for employment without regard to their race, color, religion, sex, sexual orientation, gender identity, national origin, ancestry, citizenship, age, veteran status, genetic information, physical or mental disability, medical condition, marital status, or any other basis prohibited by law.
**Red Hat does not seek or accept unsolicited resumes or CVs from recruitment agencies. We are not responsible for, and will not pay, any fees, commissions, or any other payment related to unsolicited resumes or CVs except as required in a written contract between Red Hat and the recruitment agency or party requesting payment of a fee.**
**Red Hat supports individuals with disabilities and provides reasonable accommodations to job applicants. If you need assistance completing our online job application, email** ** ** **. General inquiries, such as those regarding the status of a job application, will not receive a reply.**
We are currently looking for Technical Writing interns to join us in Boston, MA or Raleigh, NC. You will work closely with a senior mentor to gain technical knowledge and experience in your field, and cooperate with a broader international team both locally and globally. As a Technical Writer, you'll assist in the creation of feature documentation, user guides, and premium content that accompany our solutions. You will also work on effective scoping, quality testing, and delivery of writing projects, maintain a customer focus by participating in existing programs, and grow your technical expertise and strength.
In this role, you will work in an environment where different perspectives are invited, the best ideas are valued, and people feel empowered to contribute. Freedom and courage are two of our core values, which is why you can practice taking risks and exploring the unknown and developing strengths. Yet being a Red Hatter isn't just about being brave; it's also about demonstrating commitment and sticking to it.
The focus for Red Hat's Intern Program is a dual partnership between the Emerging Talent Team, and our intern managers. We can offer you professional development, social engagement and networking, performance and development, and meaningful work throughout your time at Red Hat.
**Job Responsibilities:**
+ Work closely with content strategists, engineering project teams, technical writers, and other stakeholders to produce and maintain high-quality documentation for upcoming Red Hat solution releases.
+ Engage and collaborate with the closed-loop customer feedback program to address content gaps, act on direct customer feedback, and promote continuous improvement on the documentation experience.
+ Effectively manage documentation projects and deliver customer-focused documentation
+ Gain expertise in the use of our internal documentation toolchain, including the publishing platform and issue tracking tools
+ Network with other talented interns in an inclusive workplace where you can be yourself and thrive
**Required Skills:**
+ Excellent written and verbal communication skills in English
+ Ability to read, write, and compile technical documents, including feature descriptions, customer use cases, and release notes
+ Ability to effectively establish and maintain communication with subject matter experts and other project team members.
+ Passion, curiosity, and desire to create new things and examine how things work internally
+ Willingness to learn and proactivity work as a part of a wider team
**About Red Hat**
Red Hat ( is the world's leading provider of enterprise open source ( software solutions, using a community-powered approach to deliver high-performing Linux, cloud, container, and Kubernetes technologies. Spread across 40+ countries, our associates work flexibly across work environments, from in-office, to office-flex, to fully remote, depending on the requirements of their role. Red Hatters are encouraged to bring their best ideas, no matter their title or tenure. We're a leader in open source because of our open and inclusive environment. We hire creative, passionate people ready to contribute their ideas, help solve complex problems, and make an impact.
**Inclusion at Red Hat**
Red Hat's culture is built on the open source principles of transparency, collaboration, and inclusion, where the best ideas can come from anywhere and anyone. When this is realized, it empowers people from different backgrounds, perspectives, and experiences to come together to share ideas, challenge the status quo, and drive innovation. Our aspiration is that everyone experiences this culture with equal opportunity and access, and that all voices are not only heard but also celebrated. We hope you will join our celebration, and we welcome and encourage applicants from all the beautiful dimensions that compose our global village.
**Equal Opportunity Policy (EEO)**
Red Hat is proud to be an equal opportunity workplace and an affirmative action employer. We review applications for employment without regard to their race, color, religion, sex, sexual orientation, gender identity, national origin, ancestry, citizenship, age, veteran status, genetic information, physical or mental disability, medical condition, marital status, or any other basis prohibited by law.
**Red Hat does not seek or accept unsolicited resumes or CVs from recruitment agencies. We are not responsible for, and will not pay, any fees, commissions, or any other payment related to unsolicited resumes or CVs except as required in a written contract between Red Hat and the recruitment agency or party requesting payment of a fee.**
**Red Hat supports individuals with disabilities and provides reasonable accommodations to job applicants. If you need assistance completing our online job application, email** ** ** **. General inquiries, such as those regarding the status of a job application, will not receive a reply.**
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