1,261 Medical Communication jobs in the United States

Senior Manager, Global Medical Affairs - Senior Manager, Global Medical Strategy & Communication

90407 Santa Monica, California Gilead Sciences, Inc.

Posted 2 days ago

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Job Description

We're here for one reason and one reason only - to cure cancer. Every moment is dedicated to developing treatments and every action moves us one step closer to our goal. We've made incredible scientific breakthroughs and our pioneering personalized CAR T-cell therapies have changed the paradigm. But we're not finished yet.
Join Kite, as we make even bigger advances in cancer therapies, and help shape where our business and medical science goes next.
We believe every employee deserves a great leader. People Leaders are the cornerstone to the employee experience at Gilead and Kite. As a people leader now or in the future, you are the key driver in evolving our culture and creating an environment where every employee feels included, developed and empowered to fulfil their aspirations. Join Kite and help create more tomorrows.
**Job Description**
An exciting opportunity has arisen to join the Global Medical Strategy Team with a focus on Multiple Myeloma. In this role, you will have an opportunity to be part of one an impactful medical advancement in patient care and work towards better outcomes for patients with hematological malignancies.
Your focus will be to partner with the Global Medical Multiple Myeloma Strategy Lead and be responsible for a range of key projects that are aligned to business needs. The Senior Manager will be responsible for the Medical Review of Promotional and/or Medical Affairs materials to ensure the communication is accurate, consistent, and aligned. You will be empowered to serve as an internal medical expert on medical review for promotion or drug products.
These could include but not be limited to strategic development and overall tactical implementation of Medical Affairs activities related to the lifecycle management of the product & where relevant early and late-stage pipeline launch indications. This role will report to the Global Medical Affairs Strategy lead and will work in partnership with the Multiple Myeloma team to perform all aspects of the role.
**Roles & Responsibilities:**
+ Communicates and collaborates effectively with cross-functional teams to cultivate a positive relationship
+ Provide medical review to ensure statements are scientifically valid and accurate, truthful and not misleading, and promotional claims are scientifically supported including, appropriateness of references cited
+ Provide solution oriented feedback and work collaboratively with cross-functional team members such as: legal, regulatory, marketing
+ Fully comply with Kite/Gilead policies and applicable laws, regulations and ethical standards, and make decisions within guidelines and policies
+ Maintains therapeutic area and product knowledge through ongoing assessment of relevant published literature, treatment guidelines, internal resources and data
**Skills and Competencies:**
+ Strong operational capabilities, detail oriented and commitment to advance and adhere to processes
+ Able to network with internal and partner stakeholders embracing cross-functional collaboration in a compliant manner
+ Strong analytical and problem-solving skills, with an ability to evaluate scientific data and medical literature
+ Ability to work well in a team and collaborate in a complex matrix environment
+ Ability to critically evaluate literature, interpret complex data, clear communication (written and verbal), able to articulate information to a variety of audiences and negotiate with counterparts from cross-functional areas with a solution oriented approach
+ Completes work in accordance with regulatory requirements and industry standards
**Basic Qualifications:**
Doctorate Degree and 2+ years of medical affairs or oncology experience
OR
Master's Degree and 6+ years of medical affairs or oncology experience OR
Bachelor's Degree and 8+ years of medical affairs or oncology experience
**Preferred Qualifications:**
+ Advanced Medical/Life Science degree (M.D., Pharm. D, PhD or qualification in Life Sciences, Immunology, or Oncology)
+ Relevant experience in the pharmaceutical industry, ideally with an expertise in cell therapy and Multiple Myeloma
+ Demonstrated experience within Medical Affairs with emphasis on content management systems (Veeva Vault or similar)
+ Excellent communication skills
+ Sound organizational skills to manage multiple projects simultaneously
+ Excellent written and verbal communication skills along with excellent judgment and ability to work in a team environment
+ Demonstrated ability to work across a cross functional matrix
+ Self-starter with "can do" attitude
+ Able to travel to domestic and international conferences (travel 20%)
The salary range for this position is: $153,935.00 - $199,210.00. Kite considers a variety of factors when determining base compensation, including experience, qualifications, and geographic location. These considerations mean actual compensation will vary. This position may also be eligible for a discretionary annual bonus, discretionary stock-based long-term incentives (eligibility may vary based on role), paid time off, and a benefits package. Benefits include company-sponsored medical, dental, vision, and life insurance plans*.
For additional benefits information, visit:
Eligible employees may participate in benefit plans, subject to the terms and conditions of the applicable plans.
Kite is a biopharmaceutical company engaged in the development of innovative cancer immunotherapies with a goal of providing rapid, long-term durable response and eliminating the burden of chronic care. The company is focused on chimeric antigen receptor (CAR) and T cell receptor (TCR) engineered cell therapies designed to empower the immune system's ability to recognize and kill tumors. Kite is based in Santa Monica, CA. For more information on Kite, please visit . Sign up to follow @KitePharma on Twitter at .
**For jobs in the United States:**
Gilead Sciences Inc. is committed to providing equal employment opportunities to all employees and applicants for employment, and is dedicated to fostering an inclusive work environment comprised of diverse perspectives, backgrounds, and experiences. Employment decisions regarding recruitment and selection will be made without discrimination based on race, color, religion, national origin, sex, age, sexual orientation, physical or mental disability, genetic information or characteristic, gender identity and expression, veteran status, or other non-job related characteristics or other prohibited grounds specified in applicable federal, state and local laws. In order to ensure reasonable accommodation for individuals protected by Section 503 of the Rehabilitation Act of 1973, the Vietnam Era Veterans' Readjustment Act of 1974, and Title I of the Americans with Disabilities Act of 1990, applicants who require accommodation in the job application process may contact for assistance.
For more information about equal employment opportunity protections, please view the 'Know Your Rights' ( poster.
NOTICE: EMPLOYEE POLYGRAPH PROTECTION ACT ( RIGHTS UNDER THE FAMILY AND MEDICAL LEAVE ACT
PAY TRANSPARENCY NONDISCRIMINATION PROVISION ( environment respects individual differences and recognizes each employee as an integral member of our company. Our workforce reflects these values and celebrates the individuals who make up our growing team.
Gilead provides a work environment free of harassment and prohibited conduct. We promote and support individual differences and diversity of thoughts and opinion.
**For Current Kite Pharma Employees and Contractors:**
Please apply via the Internal Career Opportunities portal in Workday.
**Change The World With Us**
Everyone at Kite is grounded by one common goal - curing cancer. Every day, we aim to establish a direct line between that purpose and our day-to-day work.
We are creating Kite together, with the recognition that the best teams are built by the best people. We maintain an attitude of curiosity, and creativity with each challenge as we develop a new market for cancer therapies. We appreciate and respect one another, and most importantly, we don't take success for granted.
While we've come a long way to make what others viewed as impossible, possible, we know one thing is certain. Today is just the beginning.
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Director, Medical Affairs

08544 Princeton, New Jersey Abbott

Posted 1 day ago

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Job Description

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues serve people in more than 160 countries.
**Director, Medical Affairs**
**Abbott is a global healthcare leader, creating breakthrough science to improve people's health. We're always looking towards the future, anticipating changes in medical science and technology.**
**Abbott Point of Care is a global leader in providing critical medical diagnostic and data management products for rapid blood analysis that are intuitive, reliable, and cost-effective. Our i-STAT System is an advanced, portable diagnostic tool that provides real-time, lab-quality results within minutes to accelerate patient-care decision-making. The i-STAT System has the industry's most comprehensive menu of tests in a single platform, including tests for blood gases, electrolytes, chemistries, coagulation, hematology, glucose, cardiac markers, and traumatic brain injury. By delivering lab-quality results in minutes, our i-STAT System fosters a collaborative, patient-centered environment while driving improved operational performance.**
**Our location in Princeton, NJ currently has an opportunity for a Director of Medical Affairs, Americas. The Director of Medical Affairs, Americas oversees the day-to-day running of, and strategic leadership for, the Medical Sciences Liaison (MSL) team, as well as representing Medical Affairs internally & externally. The MSL team members each have specific roles geographically, acting as liaisons between the commercial team and clinicians/customers for the entire Point of Care portfolio.**
**Working at Abbott**
**At Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self and live a full life. You'll also have access to:**
**Career development with an international company where you can grow the career you dream of .**
**Free medical coverage for employees* via the Health Investment Plan (HIP) PPO**
**An excellent retirement savings plan with high employer contribution**
**Tuition reimbursement, the Freedom 2 Save ( student debt program and FreeU ( education benefit - an affordable and convenient path to getting a bachelor's degree.**
**A company recognized as a great place to work in dozens of countries around the world and named one of the most admired companies in the world by Fortune.**
**A company that is recognized as one of the best big companies to work for as well as a best place to work for diversity, working mothers, female executives, and scientists.**
**What You'll Work On**
**Reporting directly to the Sr. Director, Global Medical & Scientific Affairs (GMSA), Abbott Point of Care**
**Contribution to global Medical & Scientific Affairs strategy in conjunction with Directors of EMEA and APAC Medical Affairs**
**People and project management: Ensures MSL team members update and maintain all required databases with current and complete information, including appropriate documentation of customer interactions and responses to medical information requests and/or unsolicited off-label** **inquiries/discussions.**
**Management of Medical Affairs activities within assigned budget, appropriately allocating resources as requested to support Abbott and APOC business key initiatives**
**Insuring the cross functional integration of the MSL team at the field level to maximize execution of strategic initiatives. · Ensures team member adherence to regulatory and compliance guidelines in all aspects of scientific dissemination of information**
**Cross-functional** **collaboration/interaction** **with Clinical Affairs, R&D, Regulatory, Quality, OEC, Legal, Global Marketing & Commercial teams**
**Understanding of, and respect for, different viewpoints from the perspective of both internal and external** **stakeholders/customers** **and ability to manage and resolve conflict**
**Support for the Sr. Director of GMSA, including representing Medical Affairs & the company at professional medical congresses and/or stakeholder groups as required by the function, including internal and external presentations (e.g. to HCPs, IDNs, etc.)**
**Support for the Marketing and Commercial teams regarding the medical and clinical details pertaining to the APOC portfolio and responsible for the development of activities to promote medical education within the area, particularly to help support the commercial launches of the TBI biomarker test & high-sensitivity troponin assay**
**Creation of up-to-date clinical/medical content required for internal or external education surrounding products in the portfolio or disease state awareness, as well as review/approval of ad promo materials or other assets which require** **medical/legal/regulatory** **review**
**Organization & moderation of periodic Medical Advisory Boards in conjunction with cross-functional stakeholders**
**Management of budget associated with role, including approval of MSL team expense reports**
**Assisting the Sr. Director of GMSA in the translation of educational programs established by leadership into operational plans and schedules, with well-defined KPIs and metrics aligned with the key initiatives established by the APOC Leadership Team**
**Supporting the Director of Global Scientific Affairs, in conjunction with the Sr. Manager and Project Manager in Global Scientific Affairs, with KOL management as it relates to** **investigator-sponsored** **studies (ISS) and/or collaborative research studies (CRS)**
**EDUCATION AND EXPERIENCE, YOU'LL BRING**
**MD, DO, and/or PhD degree, Emergency Medicine preferred, internal medicine, or critical care**
**Minimum 10 years' experience with a combination of residency, direct patient care experience (3 years after residency), and industry experience (5 years' experience)**
**Proven communication and presentation skills (including from the podium at scientific meetings).**
**Ability to interpret clinical data and scientific information to accurately and effectively present information to HCPs/Customers, including a commitment to build and maintain effective communication across cross-functional teams**
**Management and Organization Skills: Proactively seeks to develop and implement new ideas or solutions without prompting and shares those ideas with the team. Possesses leadership qualities and is viewed as a leader by team members and peers. Supports change and new processes and assists other team members in the adoption and implementation of same. Effectively manages budgets and other resources. Seeks to meet or exceed expectations for individual and department goals. Can successfully lead a cross-functional or cross-divisional project.**
**Advanced MSL manager experience: Consistently demonstrates ethical and compliant interactions and is viewed as a role model for the MSL role by other team members. Ability to effectively communicate the MSL role to external and internal constituents. Comprehensive understanding of the compliance guidelines for industry interactions with HCP/Customers. Uses his/her experience and judgment to communicate rules of engagement to commercial teams. Advises other MSLs on best practices for effective communication with internal and external customers. Mentors and educates other MSLs on the appropriate guidance for the MSL role; serves as an advisor on compliant interactions. Offers innovative ideas and solutions to broaden the scope and impact of the MSL role. Ability to plan strategically, aligned with APOCs most recent business goals and key initiatives**
**Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives:** ** can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year**
**Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer, committed to employee diversity.**
**Connect with us at** ** **, on Facebook at** ** **and on Twitter @AbbottNews and @AbbottGlobal.**
The base pay for this position is $147,300.00 - $294,700.00. In specific locations, the pay range may vary from the range posted.
An Equal Opportunity Employer
Abbot welcomes and encourages diversity in our workforce.
We provide reasonable accommodation to qualified individuals with disabilities.
To request accommodation, please call or email
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Account Director (Medical Affairs)

02298 Boston, Massachusetts Cognite

Posted today

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In the fast-changing world in which our clients seek to deliver life-changing medicines and technology, Cognite’s dynamic and forward-thinking team drives us in our mission of bringing science to life . As an independent agency, we develop innovative communications that convey science in the most effective and engaging way possible. Cultivating partnerships regionally and globally, we focus on the transformative therapies that are inspiring the future of healthcare and the highly complex diseases they treat. The agile and forward-thinking mindset of our Client Services team ensures strong client partnerships across global, regional and local teams. Always relied upon to deliver solutions with a smile, we go above and beyond to deliver for our clients. We are looking for a passionate Account Director to join our growing Client Services team. You will be responsible for: Successfully running your designated accounts by understanding the client’s world (their goals, priorities, brand, strategy, and competition) Meticulous account planning encompassing accurate long- and short-term resourcing, financial management, and forecasting Maintaining organization and efficiency, even when managing multiple clients and initiatives Drawing upon the quality work developed to grow both organic and de novo new business Contributing to the improvement of Cognite as an agency by providing ideas and initiatives that strengthen our business With a deep interest in science and medical communications, we believe someone with the following qualities and experience could be a good match for this role: Previous experience as an Account Director within a medical communications agency or similar A solution-oriented attitude A genuine passion for science and a desire to continuously learn about and engage with projects our clients are working on Cognite’s agency principles of Quality, Commitment, Responsiveness and Togetherness define how we work alongside our clients as a valued and supportive thinking partner while working with each other as part of a united team in which everyone plays an important role. Our benefits include: Discretionary quarterly bonus scheme Discretionary annual bonus scheme 401(k) retirement plan—up to 5% employer match 20 paid vacation days per year 20 days paid sick leave per year If you are passionate about bringing science to life ,please use the link above to apply. Seniority level Seniority level Mid-Senior level Employment type Employment type Full-time Job function Job function Marketing and Science Industries Marketing Services and Public Relations and Communications Services Referrals increase your chances of interviewing at Cognite by 2x Inferred from the description for this job 401(k) Medical insurance Get notified about new Account Director jobs in Boston, MA . Sr. Regional Director, Key Accounts -East Boston, MA $175,000.00-$35,000.00 2 weeks ago Director of Strategic Accounts (Northeast) Waltham, MA 190,000.00- 240,000.00 2 weeks ago Regional Sales Director (Remote-based role) Part-Time Director of Conference Sponsorship Sales & Corporate Relations Boston, MA 240,000.00- 300,000.00 8 hours ago Boston, MA 160,000.00- 200,000.00 2 weeks ago Boston, MA 260,000.00- 340,000.00 2 days ago Boston, MA 250,000.00- 300,000.00 4 days ago Associate Director, Sales C-Store - Remote Acton, MA 164,250.00- 246,375.00 22 hours ago Boston, MA 150,000.00- 200,000.00 3 weeks ago Waltham, MA 190,000.00- 240,000.00 2 weeks ago Boston, MA 90,000.00- 90,000.00 2 days ago We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI. #J-18808-Ljbffr

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Senior Director, Medical Affairs

02472 Watertown, Massachusetts Kymera Therapeutics

Posted 2 days ago

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Who we are:

Kymera is a clinical-stage biotechnology company pioneering the field of targeted protein degradation (TPD) to develop medicines that address critical health problems and have the potential to dramatically improve patients' lives. Kymera is deploying TPD to address disease targets and pathways inaccessible with conventional therapeutics. Having advanced the first degrader into the clinic for immunological diseases, Kymera is focused on building an industry-leading pipeline of oral small molecule degraders to provide a new generation of convenient, highly effective therapies for patients with these conditions. Founded in 2016, Kymera has been recognized as one of Boston's top workplaces for the past several years.

How we work:
  • PIONEER : We are courageous, resilient and rigorous in our mission to improve patients' lives through our revolutionary degrader medicines.
  • COLLABORATE : We value trust + transparency from everyone. Our goals are shared, our decisions data-driven and our camaraderie genuine.
  • BELONG : We recognize our differences, inviting curiosity and inclusivity, so that our people are valued, seen, and heard.
How you'll contribute:

The Senior Director, Medical Affairs, reporting into the Vice President, Medical Affairs, is a strategic leader responsible for developing and executing medical affairs strategy across key domains, including spearheading data generation and dissemination, medical-to-medical content development, scientific publications, advisory boards, field medical training materials, congress planning, and grants and sponsorships. This role will work cross-functionally with internal stakeholders (R&D, Commercial, Regulatory, etc.) and externally with healthcare professionals, key opinion leaders (KOLs), and scientific organizations to ensure impactful and compliant medical engagement and education aligned with corporate objectives.
  • Review and interpret clinical data, communicate information to stakeholders, translate scientific findings into actionable insights, and develop and drive impactful initiatives.
  • Drive the creation and implementation of a robust and impactful scientific publication strategy, emphasizing its critical role in advancing educational outreach and aligning with company clinical objectives through manuscripts, abstracts, and posters.
  • Provide medical and scientific expertise for portfolio indications on clinical trial design, safety and effectiveness, regulatory compliance, and the development of accurate medical information for educational materials.
  • Develop and lead medical strategy and engagement at major scientific congresses including planning, scientific symposia, data presentations, and KOL engagement.
  • Lead the scientific review, development, approval, execution and communication of medical affairs sponsored or supported clinical research activities.
  • Ensure seamless coordination with internal stakeholders and external agencies for logistics and deliverables across responsible functions.
  • Oversee the review, approval, and tracking of medical education grants, sponsorships, and collaborations with external scientific organizations.
  • Develop internal training and education initiatives to enhance scientific knowledge across the organization.
  • Support corporate strategy and business development by providing medical affairs input for future business opportunities.
Skills and experience you'll bring:
  • Advanced degree (MD, PharmD, PhD) in a scientific or clinical discipline required. Immunology experience strongly preferred.
  • Minimum 10+ years of experience in medical affairs roles within the pharmaceutical or biotech industry.
  • Experience developing then driving impactful medical affairs data generation and dissemination strategies based on clinical trial data, market dynamics, corporate objectives, and healthcare provider educational needs.
  • Clear understanding of clinical research methodologies and ability to independently evaluate and translate scientific material in an effective credible manner.
  • Solid understanding of clinical trial design, global drug development, regulatory approval process, and registry implementation to support clinical development programs.
  • Strong business acumen and understanding of immunology/inflammation market dynamics and key value drivers.
  • Knowledge of latest digital channels/tools to optimize education of and interactions with healthcare providers, advocacy organizations, patients, and key partners.
  • Direct knowledge of promotional regulatory processes, Fair Market Value (FMV) process, tiering, and alignment with third-party vendors.
  • In-depth knowledge of compliance, regulatory, and industry standards.
  • Exceptional leadership, project management, and strategic thinking abilities.
  • Excellent communication, presentation, and interpersonal skills.

Kymera Therapeutics is proud to be an equal opportunity employer, seeking to create a welcoming and diverse environment. All applicants will receive consideration for employment without regard to race, color, religion, creed, gender, national origin, age, disability, veteran status, pregnancy, sex, marital status, gender expression or identity, genetic information, sexual orientation, citizenship, or any other legally protected class.
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Senior Director, Medical Affairs

98213 Everett, Washington Edwards Lifesciences

Posted 3 days ago

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Patients are at the heart of everything we do. As the Senior Director, THV Medical Affairs, you will drive strategy development, evidence generation initiatives, and scientific communication activities to advance key organizational objectives that positively 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. Aortic stenosis impacts millions of people globally, yet it often remains under-diagnosed and under-treated. Edwards' groundbreaking work in transcatheter aortic heart valve replacement (TAVR) pioneered an innovative, life-changing solution for patients by offering heart valve replacement without the need for open heart surgery. Our Transcatheter Heart Valve (THV) business unit continues to partner with cardiologists and clinical teams to transform patient care with devices supported by clinical evidence. It's our driving force to help patients live longer and healthier lives. Join us and be part of our inspiring journey. **You will make an impact by.** + Leading the development and execution of strategies to address key evidence gaps and support expanded indications in alignment with the overall mission and vision of the organization + Facilitating effective collaboration across senior leadership stakeholders, including clinical, regulatory, marketing, health economics and outcomes research teams ensuring seamless integration of medical affairs initiatives into broader organizational efforts. + Building and maintaining strong relationships with external partners, including key scientific thought leaders to gather insights and collaborate on mutual goals + Managing and inspiring a team responsible for generating impactful new data using large real world data sets in collaboration with external experts (e.g., physician investigators, KOLs), driving visibility and influence + Providing strategic direction and supervisory oversight to Biostatisticians and data programmers to achieve timely and accurate data generation and analysis + Planning and directing podium and publication efforts in collaboration with internal teams and external experts to amplify Edwards' scientific presence at major conferences + Serving as strategic thought partner to Physician training team by identifying and leading new content creation for KOL speaker programs + Leading medical information efforts including managing and responding to disease and product information requests from internal and external stakeholders + Analyzing complex data, formulate strategic recommendations, and deliver high-impact communications to executive leadership + Maintaining deep scientific and product knowledge of the structural heart disease space, and distill key insights to inform strategy + Overseeing, planning, staffing, budgeting, managing expense priorities, recommending and implementing changes to methods. + Developing a robust talent development plan in alignment with the department's long-term growth strategy **What you'll need (Required):** + Advanced degree (e.g., Master's, PhD, MD) in a related field, plus professional leadership experience in the clinical, research, or healthcare industry + Extensive experience in evidence generation, development of scientific/medical conference proceedings and manuscript publication in major scientific journals + Demonstrated track record in people management **Position Location and Travel Requirements:** + This role may be based onsite at our Irvine, California campus or remote within the US, with frequent travel to the Irvine office required **What else we look for (Preferred):** + Experience working in a regulated industry + Expert scientific acumen, applied across diverse scenarios, including collaboration with internal stakeholders and physicians to identify evidence gaps and opportunities + Proven successful project management leadership skills + Excellent problem-solving, organizational, analytical and critical thinking skills including high discretion/judgment in decision making + Excellent written and verbal communication skills and interpersonal relationship skills including negotiating and relationship management skills with ability to drive achievement of objectives + Ability to work and excel within a fast paced, dynamic, and constantly changing work environment + Frequently interacts with internal and external management and senior-level stakeholders concerning projects, operational decisions, scheduling requirements, and/or contractual clarifications + Develop peer, cross functional and cross business relationships to maximize best practice sharing and team effectiveness + Provide leadership and direction to cross-functional teams to successfully implement global enterprise systems and related solutions + Adhere to all company rules and requirements (e.g., pandemic protocols, Environmental Health & Safety rules) and take adequate control measures in preventing injuries to themselves and others as well as to the protection of environment and prevention of pollution under their span of influence/control 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, the base pay range for this position is $204,000 to $289,000 (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.

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Senior Director, Medical Affairs

40601 Frankfort, Kentucky Edwards Lifesciences

Posted 3 days ago

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Job Description

Patients are at the heart of everything we do. As the Senior Director, THV Medical Affairs, you will drive strategy development, evidence generation initiatives, and scientific communication activities to advance key organizational objectives that positively 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. Aortic stenosis impacts millions of people globally, yet it often remains under-diagnosed and under-treated. Edwards' groundbreaking work in transcatheter aortic heart valve replacement (TAVR) pioneered an innovative, life-changing solution for patients by offering heart valve replacement without the need for open heart surgery. Our Transcatheter Heart Valve (THV) business unit continues to partner with cardiologists and clinical teams to transform patient care with devices supported by clinical evidence. It's our driving force to help patients live longer and healthier lives. Join us and be part of our inspiring journey. **You will make an impact by.** + Leading the development and execution of strategies to address key evidence gaps and support expanded indications in alignment with the overall mission and vision of the organization + Facilitating effective collaboration across senior leadership stakeholders, including clinical, regulatory, marketing, health economics and outcomes research teams ensuring seamless integration of medical affairs initiatives into broader organizational efforts. + Building and maintaining strong relationships with external partners, including key scientific thought leaders to gather insights and collaborate on mutual goals + Managing and inspiring a team responsible for generating impactful new data using large real world data sets in collaboration with external experts (e.g., physician investigators, KOLs), driving visibility and influence + Providing strategic direction and supervisory oversight to Biostatisticians and data programmers to achieve timely and accurate data generation and analysis + Planning and directing podium and publication efforts in collaboration with internal teams and external experts to amplify Edwards' scientific presence at major conferences + Serving as strategic thought partner to Physician training team by identifying and leading new content creation for KOL speaker programs + Leading medical information efforts including managing and responding to disease and product information requests from internal and external stakeholders + Analyzing complex data, formulate strategic recommendations, and deliver high-impact communications to executive leadership + Maintaining deep scientific and product knowledge of the structural heart disease space, and distill key insights to inform strategy + Overseeing, planning, staffing, budgeting, managing expense priorities, recommending and implementing changes to methods. + Developing a robust talent development plan in alignment with the department's long-term growth strategy **What you'll need (Required):** + Advanced degree (e.g., Master's, PhD, MD) in a related field, plus professional leadership experience in the clinical, research, or healthcare industry + Extensive experience in evidence generation, development of scientific/medical conference proceedings and manuscript publication in major scientific journals + Demonstrated track record in people management **Position Location and Travel Requirements:** + This role may be based onsite at our Irvine, California campus or remote within the US, with frequent travel to the Irvine office required **What else we look for (Preferred):** + Experience working in a regulated industry + Expert scientific acumen, applied across diverse scenarios, including collaboration with internal stakeholders and physicians to identify evidence gaps and opportunities + Proven successful project management leadership skills + Excellent problem-solving, organizational, analytical and critical thinking skills including high discretion/judgment in decision making + Excellent written and verbal communication skills and interpersonal relationship skills including negotiating and relationship management skills with ability to drive achievement of objectives + Ability to work and excel within a fast paced, dynamic, and constantly changing work environment + Frequently interacts with internal and external management and senior-level stakeholders concerning projects, operational decisions, scheduling requirements, and/or contractual clarifications + Develop peer, cross functional and cross business relationships to maximize best practice sharing and team effectiveness + Provide leadership and direction to cross-functional teams to successfully implement global enterprise systems and related solutions + Adhere to all company rules and requirements (e.g., pandemic protocols, Environmental Health & Safety rules) and take adequate control measures in preventing injuries to themselves and others as well as to the protection of environment and prevention of pollution under their span of influence/control 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, the base pay range for this position is $204,000 to $289,000 (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.

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Senior Director, Medical Affairs

55130 Minnesota, Minnesota Edwards Lifesciences

Posted 3 days ago

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Job Description

Patients are at the heart of everything we do. As the Senior Director, THV Medical Affairs, you will drive strategy development, evidence generation initiatives, and scientific communication activities to advance key organizational objectives that positively 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. Aortic stenosis impacts millions of people globally, yet it often remains under-diagnosed and under-treated. Edwards' groundbreaking work in transcatheter aortic heart valve replacement (TAVR) pioneered an innovative, life-changing solution for patients by offering heart valve replacement without the need for open heart surgery. Our Transcatheter Heart Valve (THV) business unit continues to partner with cardiologists and clinical teams to transform patient care with devices supported by clinical evidence. It's our driving force to help patients live longer and healthier lives. Join us and be part of our inspiring journey. **You will make an impact by.** + Leading the development and execution of strategies to address key evidence gaps and support expanded indications in alignment with the overall mission and vision of the organization + Facilitating effective collaboration across senior leadership stakeholders, including clinical, regulatory, marketing, health economics and outcomes research teams ensuring seamless integration of medical affairs initiatives into broader organizational efforts. + Building and maintaining strong relationships with external partners, including key scientific thought leaders to gather insights and collaborate on mutual goals + Managing and inspiring a team responsible for generating impactful new data using large real world data sets in collaboration with external experts (e.g., physician investigators, KOLs), driving visibility and influence + Providing strategic direction and supervisory oversight to Biostatisticians and data programmers to achieve timely and accurate data generation and analysis + Planning and directing podium and publication efforts in collaboration with internal teams and external experts to amplify Edwards' scientific presence at major conferences + Serving as strategic thought partner to Physician training team by identifying and leading new content creation for KOL speaker programs + Leading medical information efforts including managing and responding to disease and product information requests from internal and external stakeholders + Analyzing complex data, formulate strategic recommendations, and deliver high-impact communications to executive leadership + Maintaining deep scientific and product knowledge of the structural heart disease space, and distill key insights to inform strategy + Overseeing, planning, staffing, budgeting, managing expense priorities, recommending and implementing changes to methods. + Developing a robust talent development plan in alignment with the department's long-term growth strategy **What you'll need (Required):** + Advanced degree (e.g., Master's, PhD, MD) in a related field, plus professional leadership experience in the clinical, research, or healthcare industry + Extensive experience in evidence generation, development of scientific/medical conference proceedings and manuscript publication in major scientific journals + Demonstrated track record in people management **Position Location and Travel Requirements:** + This role may be based onsite at our Irvine, California campus or remote within the US, with frequent travel to the Irvine office required **What else we look for (Preferred):** + Experience working in a regulated industry + Expert scientific acumen, applied across diverse scenarios, including collaboration with internal stakeholders and physicians to identify evidence gaps and opportunities + Proven successful project management leadership skills + Excellent problem-solving, organizational, analytical and critical thinking skills including high discretion/judgment in decision making + Excellent written and verbal communication skills and interpersonal relationship skills including negotiating and relationship management skills with ability to drive achievement of objectives + Ability to work and excel within a fast paced, dynamic, and constantly changing work environment + Frequently interacts with internal and external management and senior-level stakeholders concerning projects, operational decisions, scheduling requirements, and/or contractual clarifications + Develop peer, cross functional and cross business relationships to maximize best practice sharing and team effectiveness + Provide leadership and direction to cross-functional teams to successfully implement global enterprise systems and related solutions + Adhere to all company rules and requirements (e.g., pandemic protocols, Environmental Health & Safety rules) and take adequate control measures in preventing injuries to themselves and others as well as to the protection of environment and prevention of pollution under their span of influence/control 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, the base pay range for this position is $204,000 to $289,000 (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.

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Senior Director, Medical Affairs

87101 Carnuel, New Mexico Edwards Lifesciences

Posted 3 days ago

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Job Description

Patients are at the heart of everything we do. As the Senior Director, THV Medical Affairs, you will drive strategy development, evidence generation initiatives, and scientific communication activities to advance key organizational objectives that positively 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. Aortic stenosis impacts millions of people globally, yet it often remains under-diagnosed and under-treated. Edwards' groundbreaking work in transcatheter aortic heart valve replacement (TAVR) pioneered an innovative, life-changing solution for patients by offering heart valve replacement without the need for open heart surgery. Our Transcatheter Heart Valve (THV) business unit continues to partner with cardiologists and clinical teams to transform patient care with devices supported by clinical evidence. It's our driving force to help patients live longer and healthier lives. Join us and be part of our inspiring journey. **You will make an impact by.** + Leading the development and execution of strategies to address key evidence gaps and support expanded indications in alignment with the overall mission and vision of the organization + Facilitating effective collaboration across senior leadership stakeholders, including clinical, regulatory, marketing, health economics and outcomes research teams ensuring seamless integration of medical affairs initiatives into broader organizational efforts. + Building and maintaining strong relationships with external partners, including key scientific thought leaders to gather insights and collaborate on mutual goals + Managing and inspiring a team responsible for generating impactful new data using large real world data sets in collaboration with external experts (e.g., physician investigators, KOLs), driving visibility and influence + Providing strategic direction and supervisory oversight to Biostatisticians and data programmers to achieve timely and accurate data generation and analysis + Planning and directing podium and publication efforts in collaboration with internal teams and external experts to amplify Edwards' scientific presence at major conferences + Serving as strategic thought partner to Physician training team by identifying and leading new content creation for KOL speaker programs + Leading medical information efforts including managing and responding to disease and product information requests from internal and external stakeholders + Analyzing complex data, formulate strategic recommendations, and deliver high-impact communications to executive leadership + Maintaining deep scientific and product knowledge of the structural heart disease space, and distill key insights to inform strategy + Overseeing, planning, staffing, budgeting, managing expense priorities, recommending and implementing changes to methods. + Developing a robust talent development plan in alignment with the department's long-term growth strategy **What you'll need (Required):** + Advanced degree (e.g., Master's, PhD, MD) in a related field, plus professional leadership experience in the clinical, research, or healthcare industry + Extensive experience in evidence generation, development of scientific/medical conference proceedings and manuscript publication in major scientific journals + Demonstrated track record in people management **Position Location and Travel Requirements:** + This role may be based onsite at our Irvine, California campus or remote within the US, with frequent travel to the Irvine office required **What else we look for (Preferred):** + Experience working in a regulated industry + Expert scientific acumen, applied across diverse scenarios, including collaboration with internal stakeholders and physicians to identify evidence gaps and opportunities + Proven successful project management leadership skills + Excellent problem-solving, organizational, analytical and critical thinking skills including high discretion/judgment in decision making + Excellent written and verbal communication skills and interpersonal relationship skills including negotiating and relationship management skills with ability to drive achievement of objectives + Ability to work and excel within a fast paced, dynamic, and constantly changing work environment + Frequently interacts with internal and external management and senior-level stakeholders concerning projects, operational decisions, scheduling requirements, and/or contractual clarifications + Develop peer, cross functional and cross business relationships to maximize best practice sharing and team effectiveness + Provide leadership and direction to cross-functional teams to successfully implement global enterprise systems and related solutions + Adhere to all company rules and requirements (e.g., pandemic protocols, Environmental Health & Safety rules) and take adequate control measures in preventing injuries to themselves and others as well as to the protection of environment and prevention of pollution under their span of influence/control 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, the base pay range for this position is $204,000 to $289,000 (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.

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Senior Director, Medical Affairs

36136 Montgomery, Alabama Edwards Lifesciences

Posted 3 days ago

Job Viewed

Tap Again To Close

Job Description

Patients are at the heart of everything we do. As the Senior Director, THV Medical Affairs, you will drive strategy development, evidence generation initiatives, and scientific communication activities to advance key organizational objectives that positively 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. Aortic stenosis impacts millions of people globally, yet it often remains under-diagnosed and under-treated. Edwards' groundbreaking work in transcatheter aortic heart valve replacement (TAVR) pioneered an innovative, life-changing solution for patients by offering heart valve replacement without the need for open heart surgery. Our Transcatheter Heart Valve (THV) business unit continues to partner with cardiologists and clinical teams to transform patient care with devices supported by clinical evidence. It's our driving force to help patients live longer and healthier lives. Join us and be part of our inspiring journey. **You will make an impact by.** + Leading the development and execution of strategies to address key evidence gaps and support expanded indications in alignment with the overall mission and vision of the organization + Facilitating effective collaboration across senior leadership stakeholders, including clinical, regulatory, marketing, health economics and outcomes research teams ensuring seamless integration of medical affairs initiatives into broader organizational efforts. + Building and maintaining strong relationships with external partners, including key scientific thought leaders to gather insights and collaborate on mutual goals + Managing and inspiring a team responsible for generating impactful new data using large real world data sets in collaboration with external experts (e.g., physician investigators, KOLs), driving visibility and influence + Providing strategic direction and supervisory oversight to Biostatisticians and data programmers to achieve timely and accurate data generation and analysis + Planning and directing podium and publication efforts in collaboration with internal teams and external experts to amplify Edwards' scientific presence at major conferences + Serving as strategic thought partner to Physician training team by identifying and leading new content creation for KOL speaker programs + Leading medical information efforts including managing and responding to disease and product information requests from internal and external stakeholders + Analyzing complex data, formulate strategic recommendations, and deliver high-impact communications to executive leadership + Maintaining deep scientific and product knowledge of the structural heart disease space, and distill key insights to inform strategy + Overseeing, planning, staffing, budgeting, managing expense priorities, recommending and implementing changes to methods. + Developing a robust talent development plan in alignment with the department's long-term growth strategy **What you'll need (Required):** + Advanced degree (e.g., Master's, PhD, MD) in a related field, plus professional leadership experience in the clinical, research, or healthcare industry + Extensive experience in evidence generation, development of scientific/medical conference proceedings and manuscript publication in major scientific journals + Demonstrated track record in people management **Position Location and Travel Requirements:** + This role may be based onsite at our Irvine, California campus or remote within the US, with frequent travel to the Irvine office required **What else we look for (Preferred):** + Experience working in a regulated industry + Expert scientific acumen, applied across diverse scenarios, including collaboration with internal stakeholders and physicians to identify evidence gaps and opportunities + Proven successful project management leadership skills + Excellent problem-solving, organizational, analytical and critical thinking skills including high discretion/judgment in decision making + Excellent written and verbal communication skills and interpersonal relationship skills including negotiating and relationship management skills with ability to drive achievement of objectives + Ability to work and excel within a fast paced, dynamic, and constantly changing work environment + Frequently interacts with internal and external management and senior-level stakeholders concerning projects, operational decisions, scheduling requirements, and/or contractual clarifications + Develop peer, cross functional and cross business relationships to maximize best practice sharing and team effectiveness + Provide leadership and direction to cross-functional teams to successfully implement global enterprise systems and related solutions + Adhere to all company rules and requirements (e.g., pandemic protocols, Environmental Health & Safety rules) and take adequate control measures in preventing injuries to themselves and others as well as to the protection of environment and prevention of pollution under their span of influence/control 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, the base pay range for this position is $204,000 to $289,000 (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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