8,486 Svar Life Science jobs in the United States

**Research Associate**
**Description**
**University of Colorado Anschutz Medical Campus**
**Department: Center for Innovative Design and Analysis (CIDA)**
**Working Title: Research Associate**
**Position #:00830009 - Requisition #:** **35848**
**Job Summary:**
**Key Responsibilities:**
+ Develop EHR-based tools and dashboards to support pulmonary research and clinical decision-making, focusing on patient demographics, treatment outcomes, and opportunities for improved care.
+ Collaborate with the Division's Biostatistics and Bioinformatics Core and Health Data Compass to maintain and optimize EHR data resources.
+ Lead and mentor junior investigators, including fellows, in the use of informatics tools and methodologies for pragmatic research.
+ Contribute to the design and execution of pragmatic clinical trials, integrating real-world data to drive evidence-based improvements in patient care.
+ Develop a collaboration research portfolio that includes involvement in preparation of grant applications, analyses, and publication of data generated from funded studies.
**Work Location:**
Hybrid
**Why Join Us:**
**Why work for the University?**
+ Medical: Multiple plan options
+ Dental: Multiple plan options
+ Additional Insurance: Disability, Life, Vision
+ Retirement 401(a) Plan: Employer contributes 10% of your gross pay
+ Paid Time Off: Accruals over the year
+ Vacation Days: 22/year (maximum accrual 352 hours)
+ Sick Days: 15/year (unlimited maximum accrual)
+ Holiday Days: 10/year
+ Tuition Benefit: Employees have access to this benefit on all CU campuses
+ ECO Pass: Reduced rate RTD Bus and light rail service
**Diversity and Equity:**
**Qualifications:**
**Minimum Qualifications:**
**Applicants must meet minimum qualifications at the time of hire.**
+ PhD in biomedical informatics, biostatistics, data science, or related discipline.
+ 1 year of working with EHR data, including data extraction, cleaning, and analysis for clinical research purposes including time during graduate studies.
+ 1 year of experience in pragmatic studies and real-world data applications including time during graduate studies.
+ Strong collaborative skills and ability to work with multidisciplinary teams.
**Preferred Qualifications:**
+ 1 year post-graduate experience working with EHR data, including data extraction, cleaning, and analysis for clinical research purposes.
+ 1 year post-graduate experience in pragmatic studies and real-world data applications.
**Knowledge, Skills and Abilities:**
+ Strong knowledge of basic statistical principles relevant in medical research.
+ Strong knowledge of EHR data architectures and ontologies.
+ Evidence of an ability to conduct methods research or investigate the validity of new methods in their area of study.
+ Evidence of developing informatics techniques or pipelines and applying them in new situations.
+ Ability to analyze and solve complex data wrangling problems.
+ Strong collaborative skills and ability to work with multidisciplinary teams.
+ Experience mentoring junior investigators or fellows.
+ Strong programming skills in multiple languages including SQL, Python, R, or others.
+ Experience with high-performance computing environments.
+ Good organizational skills across individual projects, managing own workload.
+ Positive attitude and the ability to work with a variety of biomedical investigators and colleagues.
+ Excellent problem-solving skills.
+ An innate desire to learn new methods and technologies and adapt to the demands of a fast paced and ever-evolving research environment.
+ Ability to contribute to the growth and development of the CIDA, The Division of Pulmonary, and the Department.
+ Strong written and oral communication skills, including the ability to be culturally responsive and exercise cultural humility while communicating appropriately and effectively with diverse audiences.
**How to Apply:**
1. A letter of interest describing relevant job experiences as they relate to listed job qualifications and interest in the position
2. Curriculum vitae / Resume
3. Three to five professional references, including name, address, phone number (mobile number if appropriate), and email address
**Screening of Applications Begins:**
**January 24, 2025**
**Anticipated Pay Range:**
**$90,000 - $113,630**
**ADA Statement:**
**Background Check Statement:**
**Vaccination Statement:**
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**Primary Location**
**Schedule**
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**To apply, visit ( 2025 Jobelephant.com Inc. All rights reserved.
Posted by the FREE value-added recruitment advertising agency ( Associate - 35848 Research Faculty
The Colorado School of Public Health (ColoradoSPH) has an opening for a full-time Research Associate, Biomedical Informatician position within the Research Associate track. This position will reside within the Center for Innovative Design and Analysis (CIDA) with faculty membership in the Department of Biostatistics and Informatics. This is a doctoral level team science position and similar to team science track faculty positions at other institutions. CIDA is a campus wide analytics center charged with expanding the analytics expertise and research for the Anschutz Medical Campus. The person in this position will join over three dozen master's and PhD trained faculty in CIDA and over three-dozen faculty and research personnel in the Department of Biostatistics and Informatics.The work for this position is with expertise in biomedical informatics, biostatistics, data science, or a related field. The incumbent will play a key role in developing a learning health system, leveraging electronic health record (EHR) data to support clinical research in pulmonary medicine. They will work closely with the Pulmonary Translational Biostatistics and Bioinformatics Core, Health Data Compass (the campus' EHR data warehouse), and pulmonary investigators to create tools and systems that enable near-real-time insights into patient care.The Research Associate is a key research-faculty position in the Center and Department. A Research Associate is expected to provide high-level, professional and scientifically rigorous informatics/data science collaborative support to biomedical researchers at CU Anschutz. They are expected to become a significant contributor in their collaborations, and partner to define and shape the research direction of the team. A person in this position works with investigators on the data architecture design aspects of the clinical care and research process, including: design of new instruments and data presentation, structuring data collection systems, the application of state-of-the-art informatics methodologies, and analyses. They will be involved in, and at times lead, learning health system product development including dash boards, white papers, treatment policy changes. They will also be involved in, and at times lead, traditional research products including, abstracts, oral and poster presentations, and scientific manuscripts. Depending on the particular collaborations interesting informatics /data science research opportunities may arise; although it is not the emphasis of the position.The position offers attractive career perspectives for talented and highly motivated individuals who have a passion for teaching and are motivated to contribute to highly collaborative and innovative translational and clinical research.
- this role is eligible for a hybrid schedule of 3 days per week on campus and as needed for in-person meetings.
CIDA is the campus wide analytics center and provides consulting and in-depth collaboration for researchers on the Anschutz Medical Campus and the surrounding community. CIDA builds successful collaborations with over 30 groups on campus, and have team members on more than 60 grants. The person in this position will join a curious and dynamic group of master's and doctoral trained faculty in CIDA and over three-dozen faculty and research personnel in the Department of Biostatistics and Informatics. Professional and research activities in the Department of Biostatistics and Informatics and The Center for Innovative Design and Analysis are wide ranging bridging informatics and biostatistics to create a data science motivated faculty. The faculty research is a mix of methodology and team science/collaborative work. The Colorado School of Public Health is a collaborative endeavor involving the University of Colorado Anschutz Medical Campus (CU Anschutz), Colorado State University (CSU), and the University of Northern Colorado (UNC). The Colorado School of Public Health is the first and only accredited school of public health in the Rocky Mountain Region, attracting top tier faculty and students from across the country, and providing vital contributions towards ensuring our region's health and wellbeing. Collaboratively formed in 2008 by CU Anschutz, CSU and UNC, the Colorado School of Public Health provides education programs including a Master's concentration in global health, innovative research that places the School in the top 20 in NIH funding among Schools of Public Health, and community service that addresses public health issues including chronic disease, access to healthcare, climate and environmental threats, emerging infectious diseases, population mental health, ONE HEALTH and injuries for Rocky Mountain region, nationally and globally. The School is committed to diversity and inclusion in its faculty, staff, administration, and student body. The School intentionally builds the public health infrastructure toward health equity and the elimination of health disparities for all communities. The ColoradoSPH aims to build a diverse and representative academic community that recognizes the importance of social, economic, health, and environmental justice. We strive to promote equity, diversity, and to be a model of inclusive excellence. As a tri-campus partnership, ColoradoSPH stands with academic, practice, and community partners nationwide to condemn racism, injustice, and inequity. Please click here to learn more about our equity, diversity, and inclusion commitment statement and plan to dismantle structural racism: ( . We have AMAZING benefits and offerexceptional amounts of holiday, vacation and sick leave! The University of Colorado offers an excellent benefits package including: There are many additional perks & programs with the CU Advantage ( .
The University of Colorado Anschutz Medical Campus is committed to recruiting and supporting a diverse student body, faculty and administrative staff. The university strives to promote a culture of inclusiveness, respect, communication and understanding. We encourage applications from women, ethnically minoritized individuals, persons with disabilities, persons within the LGBTQ+ community and all veterans. In addition, the Anschutz Campus has also been recognized as an Age-Friendly University. The University of Colorado is committed to diversity and equality in education and employment.
For full consideration, please submit the following document(s): Questions should be directed to: Ryan Peterson, PhD at ( will be accepted until finalists are identified, but preference will be given to complete applications received by . Those who do not apply by this date may or may not be considered.
The starting salary range for this position has been established as The above salary range (or hiring range) represents the University's good faith and reasonable estimate of the range of possible compensation at the time of posting. This position may be eligible for overtime compensation, depending on the level.Your total compensation goes beyond the number on your paycheck. The University of Colorado provides generous leave, health plans and retirement contributions that add to your bottom line.Total Compensation Calculator: ( University will provide reasonable accommodations to applicants with disabilities throughout the employment application process. To request an accommodation pursuant to the Americans with Disabilities Act, please contact the Human Resources ADA Coordinator at ( .
The University of Colorado Anschutz Medical Campus is dedicated to ensuring a safe and secure environment for our faculty, staff, students and visitors. To assist in achieving that goal, we conduct background investigations for all prospective employees.
CU Anschutz strongly encourages vaccination against the COVID-19 virus and other vaccine preventable diseases ( . If you work, visit, or volunteer in healthcare facilities or clinics operated by our affiliated hospital or clinical partners or by CU Anschutz, you will be required to comply with the vaccination and medical surveillance policies of the facilities or clinics where you work, visit, or volunteer, respectively. In addition, if you work in certain research areas or perform certain safety sensitive job duties, you must enroll in the occupational health medical surveillance program ( . Application Materials Required: Cover Letter, Resume/CV, List of References : Faculty : Aurora Department: U0001 -- Anschutz Med Campus or Denver - 21742 - CSPH-CIDA Gen Ops : Full-time : Jan 7, 2025 : Ongoing Posting Contact Name: Ryan Peterson, PhD Posting Contact Email: ( Position Number: 00830009jeid-f243865208489748b781d8831e284848
The University of Colorado does not discriminate on the basis of race, color, national origin, sex, age, pregnancy, disability, creed, religion, sexual orientation, gender identity, gender expression, veteran status, political affiliation, or political philosophy. All qualified individuals are encouraged to apply.

**Research Associate**
Science & Research
New Castle County, DE, US
Pay Rate Low: 38 | Pay Rate High: 48
+ Added - 10/02/2025
Apply for Job
We are seeking a motivated Research Associate to join a unique pre-clinical lab focused on developing CAR T cell therapies
**Responsibilities:**
+ Perform molecular biology techniques, including DNA manipulation, cloning of CAR-T cell constructs, and transduction of T-cells using lentiviral vectors.
+ Package and titer lentiviral vectors
+ Run assays like flow cytometry, ELISA to analyze experimental data.
+ Design cell constructs with improved specificity and efficacy.
+ Independently and collaboratively design and execute experiments, troubleshoot, and analyze results.
+ Maintain detailed records, contribute to reports, and assist with manuscript preparation.
+ Participate in lab maintenance, including equipment setup, troubleshooting, and ordering supplies.
+ Stay updated on relevant scientific literature and contribute to the development of SOPs.
**Qualifications:**
+ Advanced degree in related field or Bachelors and 3+ years of experience .
+ Experience in molecular and cell biology, including vector construction, transduction, and assay execution.
+ This is an onsite role that will primarily be on the bench conducting research
Pay: $40-48/hr
This job description is a complete list of all desired skills, but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you!
We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.

Job Title: Research AssociateJob Description
We are seeking a dedicated Research Associate to join our innovative team focused on microbiology and molecular biology projects. This role initially involves working on straightforward, repetitive tasks within microbiology before expanding to molecular biology projects. You will work closely with a team of scientists and engineers to design and conduct experiments, develop assays, and contribute to the automation of laboratory techniques within disposable devices.
Responsibilities
+ Conduct bacterial culturing and plating to grow bacteria.
+ Utilize UV Vis spectrophotometry to monitor and measure microbial growth.
+ Maintain good aseptic techniques and strong lab organizational skills.
+ Work with blood in a BSL-2 facility, utilizing PPE and receiving necessary training.
+ Work under the direction of a Scientist/Sr. Scientist on product development projects.
+ Design and implement experiments to develop and optimize assays on the bench and within consumable devices.
+ Take detailed notes and follow good documentation practices.
+ Summarize and communicate experimental data, drawing conclusions independently.
+ Identify and resolve assay and device performance issues.
Essential Skills
+ Proficiency in assay development, PCR, molecular biology, and bacterial culturing.
+ Experience with spectrometry, in vitro diagnostics, and nucleic acid extractions.
+ Strong knowledge of microbiology and aseptic techniques.
+ Experience with digital PCR and qPCR.
Additional Skills & Qualifications
+ BA/BS or MA/MS in life sciences with 2+ years of relevant laboratory experience.
+ Fundamental knowledge of chemistry, biochemistry, molecular biology, and immunology.
+ Strong analytical and problem-solving skills.
+ Ability to work independently and in multi-disciplinary teams.
+ Good organizational skills and appropriate computer skills (e-mail, word processing, Excel, graphing and analytic software).
+ Creative thinking and problem-solving abilities.
Work Environment
You will join a collaborative team consisting of 4-5 scientists and 4-5 engineers. Our facility in Carlsbad, CA is dedicated to in vitro diagnostic (IVD) product development and the automation of laboratory techniques within disposable devices. The work environment encourages innovation and mentorship, offering a platform for professional growth.
Job Type & Location
This is a Contract position based out of Carlsbad, California.
Pay and Benefits
The pay range for this position is $27.00 - $40.00/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
- Medical, dental & vision - Critical Illness, Accident, and Hospital - 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available - Life Insurance (Voluntary Life & AD&D for the employee and dependents) - Short and long-term disability - Health Spending Account (HSA) - Transportation benefits - Employee Assistance Program - Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in Carlsbad,CA.
Application Deadline
This position is anticipated to close on Aug 29, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email (% ) for other accommodation options.

Job Title: Research Associate
Job Description
We are seeking a Research Associate with a focus on qPCR optimization and assay development. This role involves working primarily on the bench, performing DNA extractions and PCR sequencing using blood samples. The position offers ample opportunities to learn molecular techniques and automate processes within a dynamic biotech environment.
Responsibilities
+ Perform experiments and procedures in accordance with written protocols.
+ Assist in developing protocols and procedures.
+ Document, report, and present results of experiments and procedures.
+ Follow work instructions and SOPs as required by ISO quality management systems.
+ Assist in maintaining laboratory inventory and equipment.
+ Work collaboratively within the platform integration team and cross-functionally with other teams.
+ Contribute to the success of the entire project through effective problem-solving and communication.
Essential Skills
+ 3-5 years of experience in applicable life sciences such as Molecular Biology, Biochemistry, Microbiology, Chemistry, or Immunology.
+ Proficiency in nucleic acid techniques including DNA extraction, purification, quantification, qPCR, and PCR multiplex.
+ Experience with molecular biology sample preparation using magnetic particles.
+ Competency in data interpretation and analysis.
+ Knowledge of standard laboratory techniques such as aseptic technique.
+ Ability to work with human blood samples.
+ Experience with Python is ideal as well as reading code after running PCR
Additional Skills & Qualifications
+ Bachelor's Degree in Biology, Chemistry, or other relevant field with 3-5 years of experience.
+ Master's Degree in Biology, Chemistry, or other relevant field with 1+ years industry experience.
+ Experience working in a BSL-2 environment with live organisms is a plus.
+ Competency with Microsoft Office Suite (MS Word, Excel, PowerPoint).
+ Excellent organizational and project management skills.
+ Ability to plan and execute experiments with minimal assistance.
Work Environment
The role is part of a seven-member integration team within a larger group of seventeen professionals. The work environment includes administration, laboratory, and manufacturing settings. The position requires working in the lab 90% of the time with flexible hours, starting no later than 8:30 AM. The company culture is supportive, with kind and personable colleagues, and offers flexible work times to accommodate personal needs.
Pay and Benefits
The pay range for this position is $38.50 - $38.50/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
- Medical, dental & vision - Critical Illness, Accident, and Hospital - 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available - Life Insurance (Voluntary Life & AD&D for the employee and dependents) - Short and long-term disability - Health Spending Account (HSA) - Transportation benefits - Employee Assistance Program - Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in CARLSBAD,CA.
Application Deadline
This position is anticipated to close on Aug 29, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email (% ) for other accommodation options.

Job Title: Research Associate
Job Description
We are seeking a Research Associate with a focus on qPCR optimization and assay development. This role involves working primarily on the bench, performing DNA extractions and PCR sequencing using blood samples. The position offers ample opportunities to learn molecular techniques and automate processes within a dynamic biotech environment.
Responsibilities
+ Perform experiments and procedures in accordance with written protocols.
+ Assist in developing protocols and procedures.
+ Document, report, and present results of experiments and procedures.
+ Follow work instructions and SOPs as required by ISO quality management systems.
+ Assist in maintaining laboratory inventory and equipment.
+ Work collaboratively within the platform integration team and cross-functionally with other teams.
+ Contribute to the success of the entire project through effective problem-solving and communication.
Essential Skills
+ 3-5 years of experience in applicable life sciences such as Molecular Biology, Biochemistry, Microbiology, Chemistry, or Immunology.
+ Proficiency in nucleic acid techniques including DNA extraction, purification, quantification, qPCR, and PCR multiplex.
+ Experience with molecular biology sample preparation using magnetic particles.
+ Competency in data interpretation and analysis.
+ Knowledge of standard laboratory techniques such as aseptic technique.
+ Ability to work with human blood samples.
+ Experience with Python is ideal as well as reading code after running PCR
Additional Skills & Qualifications
+ Bachelor's Degree in Biology, Chemistry, or other relevant field with 3-5 years of experience.
+ Master's Degree in Biology, Chemistry, or other relevant field with 1+ years industry experience.
+ Experience working in a BSL-2 environment with live organisms is a plus.
+ Competency with Microsoft Office Suite (MS Word, Excel, PowerPoint).
+ Excellent organizational and project management skills.
+ Ability to plan and execute experiments with minimal assistance.
Work Environment
The role is part of a seven-member integration team within a larger group of seventeen professionals. The work environment includes administration, laboratory, and manufacturing settings. The position requires working in the lab 90% of the time with flexible hours, starting no later than 8:30 AM. The company culture is supportive, with kind and personable colleagues, and offers flexible work times to accommodate personal needs.
Pay and Benefits
The pay range for this position is $38.50 - $38.50/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
- Medical, dental & vision - Critical Illness, Accident, and Hospital - 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available - Life Insurance (Voluntary Life & AD&D for the employee and dependents) - Short and long-term disability - Health Spending Account (HSA) - Transportation benefits - Employee Assistance Program - Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in CARLSBAD,CA.
Application Deadline
This position is anticipated to close on Aug 29, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email (% ) for other accommodation options.

This position supports Dr. Wu's SERA study, which investigates sex differences in Alzheimer's Disease risk and the potential impact of equol supplementation on modifying that risk. The study includes clinical, biological, and neuroimaging components, and the research team works collaboratively to collect and process data from older adult participants. The Research Associate will assist with blood processing, conduct phone screens with potential participants, enter study data, and escort participants to MRI appointments. He will play a key role in ensuring smooth day-to-day operations and maintaining data integrity across clinical and imaging components of the study.
This position is grant funded.
Responsibilities:
+ Contact and schedule potential participants from a designated pool of individuals who have agreed to be contacted for research studies.
+ Conduct subject searches to locate subjects who are unable to be contacted.
+ Explain research protocol and obtain informed consent from participants.
+ Conduct on-line and/or library searches as needed by the PI as necessary.
+ Perform phone interviews for research project protocol(s) as needed.
+ Maintain and update subject information database.
+ Conduct interviews with research participants under supervision as needed.
+ Standardize data sets and transcribe necessary data to the requirements of the study, including information collected during participant interactions.
+ Bachelors Degree in Psychology, Neuroscience, Counseling, Sociology or related research field or current enrollment in a related Bachelor's Degree program with direct experience in a research environment required.
+ Familiarity with computers and common software packages required.
+ Prior related work experience in a research setting preferred.
+ Working knowledge of research methodology strongly preferred.
**Licensure, Certifications, and Clearances:**
+ Act 34 with renewal
**UPMC is an Equal Opportunity Employer/Disability/Veteran**

Job Description
The Research Associate will collect face and body data gathered from large-scale capture domes and VR headsets by:
● Staging and setting-up equipment for the study, which may include engaging with engineering, external equipment vendors, internal and external safety evaluators, and the research study team to ensure the equipment is set up properly.
● Conducting the study, including participant coaching and interaction, operating complex, experimental capture systems, and debriefing with team leadership as necessary
● Performing basic troubleshooting of capture systems (hardware and software) and escalate any bugs or issues using internal tools.
● Providing research study support, including data collection, tracking of participants, and tracking of equipment and procedures.
● Contributing to and/or update existing documentation
● Serving as a participant for studies and being captured in various systems as needed.
● Completing project work related to captures such as recording and updating capture scripts.
● Attending all required trainings, meetings, and standups
● Providing feedback for process improvement areas
Expectations for Success
To be able to successfully execute on the day-to-day responsibilities above, the Research Associate is expected to:
● Review SOPs and other any other relevant documentation and consult with the responsible Lead for any questions or clarifications in advance of the capture.   
● Stay up to date with process and SOP changes for frequently used systems.
● Arrive on-time for captures and allow additional time, if needed, to review unfamiliar systems or SOPs and for operational set up
● Arrive on-time and prepared with relevant information or materials for all required trainings, meetings, and standups.
● Approach each capture and project with ability and flexibility. Be prepared to quickly pivot to new tasks, approaches to capture, or steps in documented processes to keep the team moving forward, even during blocking events.
● Provide a comfortable and professional experience for participants (both internal and external) through all interactions including providing updates and breaks during troubleshooting or other capture-blocking events.
● Ensure highest quality and accuracy of data captured by maintaining a sterile and distraction-free capture environment.
● Escalate any issues to the Engineer Team and properly documenting, in-detail, the nature of the issue.
● Address any areas for improvement of the capture process in scheduled meetings and/or via internal feature request tools.
● Identify (or partner with the Team Lead(s)) projects and tasks that can be completed during larger blocking events and during planned and unplanned system downtime.
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: and Requirements
- Bachelor's degree and/or at least one year of professional work experience
- Experience with research or following work processes (gathering requirements, capturing notes, documentation). Any clinical experience can work as well. Need to show that they've handled a lot of tasks at once while staying organized/not missing steps.
- Customer service experience. Ability to get people out of their comfort zone and be someone's friend for a day. This person should enjoy working with people daily.
- Strong organizational, interpersonal skills, and attention to detail
- Demonstrated ability to remain calm in stressful situations.
- Demonstrated ability to remain adaptable and flexible in stressful situations. Need to be okay with not always knowing the why behind things and understand this is an operational role.
- Demonstrated ability to proactively identify and solve problems.
- 1+ year of experience with Windows and macOS - Experience with virtual reality systems, cameras and optical systems, lighting systems, and audio systems 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

The Department of Cell and Developmental Biology at the Perelman School of Medicine at the University of Pennsylvania seeks candidates for a Research Associate position in the Academic Support Staff. This appointment will be initially for one (1) year and continuation during that time period and renewal are based on satisfactory performance and availability of funding (limited to three (3) years). Expertise is required in the specific area of IVF, mouse models, histology, epigenetics assays. Applicants must have a Ph.D. degree.
Responsibilities may include investigation of the outcomes of Assisted Reproductive Technologies using a mouse model.
The successful applicant will have an opportunity to further develop their epigenetics skills.
Candidate should have a minimum of 3-5 years postdoctoral experience.
We seek candidates who embrace and reflect diversity in the broadest sense. The University of Pennsylvania is an EOE. Minorities/women/individuals with disabilities/protected veterans are encouraged to apply.
The University of Pennsylvania is an equal opportunity employer. Candidates are considered for employment without regard to race, color, sex, sexual orientation, religion, creed, national origin (including shared ancestry or ethnic characteristics), citizenship status, age, disability, veteran status or any class protected under applicable federal, state, or local law.

**Why People choose to work at Labcorp:**
At Labcorp, it is our people that make us great - it's what our clients, our partners and, most importantly, what our employees say. Here, you will have the opportunity to collaborate with extraordinary people with diverse viewpoints. You will discover your own outstanding potential as we build an even stronger organization with industry leaders from early development to the clinic and beyond. We help our clients develop medicines that improve health and improve lives of their family and friends.
**We have an excellent career opportunity for a Research Associate to join our Metabolism team in Madison, WI.**
**Position Summary:**
The Research Associate will conduct all work in compliance with appropriate company standards, GLP, GCP, GMP (where appropriate) and regulatory guidelines specified in the study plans, protocols, or work agreements governing the work in which they are involved.
**Essential Duties:**
+ Set up and perform a variety of analyses using appropriate instrumentation with routine and non-routine methods
+ Critically review study protocol in primary areas of work and suggest changes where appropriate
+ Provides input and participates in study meetings (ie pre-initiation meeting)
+ Maintains study documentation in compliance with regulatory guidelines
+ Ability to recognize deviations from normal results and inform Study Director, Study Coordinator and/or management of any problems that may affect integrity of the data
+ Ability to recommend modifications to routine procedures to adapt to problems in primary area
+ Ability to understand the scope of a study (primary area of work) and be able to complete with no supervision
+ Deliver results within the agreed timeframe, whilst recognizing changes in priorities
+ Routinely support studies in non-primary areas of work
+ Ability to write, review and revise standard SOPs related to primary area of work.
+ Participate in QC review of selected routine data and methodology section within reports within scope of current role
+ Ability to prepare results and presentations based on the work performed
+ Evaluates data for experiment modification and contribute to report preparation/review
+ Participate in method development and validation projects
+ Maintains a clean and safe laboratory work environment and perform routine maintenance
+ Performs other related duties as assigned
**Education/Experience:**
+ Bachelor's degree in biology, chemistry or other relevant scientific discipline
+ Experience in a research or lab environment
+ Demonstrated experience in analytical chemistry is strongly preferred
+ Hands on experience with high performance liquid chromatography (HPLC) strongly preferred
+ Prior experience in pulling and processing biological samples strongly preferred
+ Must be proficient in Microsoft Office Suite (including Word, Excel, PowerPoint, and Outlook) and comfortable using or learning additional software as needed
**Benefits:** Employees regularly scheduled to work 20 or more hours per week are eligible for comprehensive benefits including: Medical, Dental, Vision, Life, STD/LTD, 401(k), Paid Time Off (PTO) or Flexible Time Off (FTO), Tuition Reimbursement and Employee Stock Purchase Plan. Casual, PRN & Part Time employees regularly scheduled to work less than 20 hours are eligible to participate in the 401(k) Plan only. For more detailed information, please click here ( **.**
**Labcorp is proud to be an Equal Opportunity Employer:**
Labcorp strives for inclusion and belonging in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications and merit of the individual. Qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. Additionally, all qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable law.
**We encourage all to apply**
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