Mid Level Epidemiologist Jobs
Mid level epidemiologist jobs go to professionals ready to take full ownership of studies, coordinate across agencies, and translate findings into public health action with limited oversight. Roles are distributed across Consulting & Professional Services, Biotechnology & Pharmaceuticals, and Education, with on-site, hybrid, and remote positions available, and employers like IQVIA, TRC Companies, and University of New Orleans hiring at this level now.
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Join IQVIA’s Sponsor-Dedicated FSP team and help advance healthcare through real-world evidence. We bring together scientific expertise and real-world data to help sponsors make decisions and accelerate evidence generation to improve patient outcomes. In this role, you’ll work closely with one sponsor, gaining deep knowledge of their therapies while leveraging IQVIA’s global expertise.
Core Function Description:
This role will support the Inflammation, Real World Evidence team, providing scientific and strategic epidemiology support for clinical development and drug safety activities. This role will leverage secondary real-world data (RWD) sources to generate evidence that informs regulatory, safety, and clinical development decisions across the product lifecycle.
Key responsibilities include designing and conducting observational research studies, assessing evidence gaps, evaluating safety profiles, and developing evidence strategies to support regulatory interactions and clinical development programs. The Senior Epidemiologist will collaborate closely with cross-functional teams, including Clinical Development, Safety, Regulatory Affairs, Biostatistics, and Real-World Evidence stakeholders, to ensure appropriate epidemiologic approaches are applied to address critical business and scientific questions.
The ideal candidate will have deep expertise in epidemiologic methods, demonstrated experience working within pharma or biotech, and a thorough understanding of regulatory requirements related to clinical development and safety evidence generation.
This is a fully remote position based in the United States.
Minimum Qualifications
Doctoral degree (PhD, ScD, or equivalent) in Epidemiology.
5 to 7 years of epidemiology experience within a pharmaceutical/biotechnology company.
Demonstrated experience supporting clinical development and/or drug safety.
Strong expertise in observational research methods and the use of commercial healthcare databases such as HealthVerity, Pharmetrics Plus, TriNetX, or similar real-world data assets.
Solid understanding of regulatory requirements and evidence needs supporting clinical development, including the generation of evidence to address regulatory questions related to safety profiles and evidence gaps for Phase II and Phase III programs.
Proven ability to design, execute, and interpret epidemiologic studies that support regulatory, clinical, or safety objectives.
Preferred Qualifications
Experience in Inflammation and Immunology therapeutic areas.
Knowledge of disease areas such as Atopic Dermatitis, Asthma, Lupus, Immune Thrombocytopenia (ITP), Autoimmune Hemolytic Anemia, or other immune-mediated diseases.
Experience supporting assets within emerging immunology programs.
Experience working with primary or hybrid real-world data sources in addition to secondary data sources.
Prior experience supporting regulatory submissions or interactions with FDA, EMA, or other global health authorities.
What’s in it for you?
Be part of a forward-thinking team that helps shape the next generation of evidence-based healthcare.
Work hand-in-hand with one leading sponsor, gaining deep expertise in their therapies.
Access IQVIA’s global network who supports your growth.
This is your chance to make an impact, while building a career that matters.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com
IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
The potential base pay range for this role, when annualized, is $109,200.00 - $273,000.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.Join IQVIA’s Sponsor-Dedicated FSP team and help advance healthcare through real-world evidence. We bring together scientific expertise and real-world data to help sponsors make decisions and accelerate evidence generation to improve patient outcomes. In this role, you’ll work closely with one sponsor, gaining deep knowledge of their therapies while leveraging IQVIA’s global expertise.
Core Function Description:
This role will support the Inflammation, Real World Evidence team, providing scientific and strategic epidemiology support for clinical development and drug safety activities. This role will leverage secondary real-world data (RWD) sources to generate evidence that informs regulatory, safety, and clinical development decisions across the product lifecycle.
Key responsibilities include designing and conducting observational research studies, assessing evidence gaps, evaluating safety profiles, and developing evidence strategies to support regulatory interactions and clinical development programs. The Senior Epidemiologist will collaborate closely with cross-functional teams, including Clinical Development, Safety, Regulatory Affairs, Biostatistics, and Real-World Evidence stakeholders, to ensure appropriate epidemiologic approaches are applied to address critical business and scientific questions.
The ideal candidate will have deep expertise in epidemiologic methods, demonstrated experience working within pharma or biotech, and a thorough understanding of regulatory requirements related to clinical development and safety evidence generation.
This is a fully remote position based in the United States.
Minimum Qualifications
Doctoral degree (PhD, ScD, or equivalent) in Epidemiology.
5 to 7 years of epidemiology experience within a pharmaceutical/biotechnology company.
Demonstrated experience supporting clinical development and/or drug safety.
Strong expertise in observational research methods and the use of commercial healthcare databases such as HealthVerity, Pharmetrics Plus, TriNetX, or similar real-world data assets.
Solid understanding of regulatory requirements and evidence needs supporting clinical development, including the generation of evidence to address regulatory questions related to safety profiles and evidence gaps for Phase II and Phase III programs.
Proven ability to design, execute, and interpret epidemiologic studies that support regulatory, clinical, or safety objectives.
Preferred Qualifications
Experience in Inflammation and Immunology therapeutic areas.
Knowledge of disease areas such as Atopic Dermatitis, Asthma, Lupus, Immune Thrombocytopenia (ITP), Autoimmune Hemolytic Anemia, or other immune-mediated diseases.
Experience supporting assets within emerging immunology programs.
Experience working with primary or hybrid real-world data sources in addition to secondary data sources.
Prior experience supporting regulatory submissions or interactions with FDA, EMA, or other global health authorities.
What’s in it for you?
Be part of a forward-thinking team that helps shape the next generation of evidence-based healthcare.
Work hand-in-hand with one leading sponsor, gaining deep expertise in their therapies.
Access IQVIA’s global network who supports your growth.
This is your chance to make an impact, while building a career that matters.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com
IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
The potential base pay range for this role, when annualized, is $109,200.00 - $273,000.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.See All 13 Mid Level Epidemiologist Jobs
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Mid Level Epidemiologist Jobs: Frequently Asked Questions
How do I get a mid level epidemiologist job?
Highlight your independent contributions: studies you designed, data you analyzed without close supervision, and findings you presented to stakeholders. Tailor your resume to show ownership rather than participation. Emphasize any specialty area you have deepened, such as infectious disease, chronic conditions, or environmental health, and demonstrate that you can move a project from protocol development through dissemination with minimal direction.
Which companies hire mid level epidemiologists?
Companies hiring mid level epidemiologists right now include IQVIA, TRC Companies, and University of New Orleans, based on current listings on Migrate Mate as of July 2026. Hiring at this level covers public health agencies, hospital systems, research universities, health insurers, and life sciences companies that need researchers who can run projects independently rather than solely support senior staff.
Are there remote mid level epidemiologist jobs?
Yes, though availability depends on the employer and the type of work involved. About 90% of mid level epidemiologist openings are remote or hybrid as of July 2026, concentrated in roles focused on data analysis, surveillance reporting, and health policy rather than fieldwork or laboratory-based investigation. Hybrid schedules are common at government agencies and large health systems.
How do I move up to a mid level epidemiologist role?
Growth into mid level comes from accumulating evidence of independent contribution over your first few years. Build depth in a specialty, volunteer to lead a component of a larger study, and document measurable outcomes like publications, policy reports, or surveillance improvements. Strengthening statistical or GIS skills, earning a relevant certification, and mentoring newer colleagues all signal readiness for broader ownership and a mid level title.
Which industries hire the most mid level epidemiologists?
Mid Level epidemiologist roles concentrate in Consulting & Professional Services, Biotechnology & Pharmaceuticals, and Education, based on current listings on Migrate Mate as of July 2026. These sectors drive demand because they require ongoing disease surveillance, outcomes research, program evaluation, and regulatory compliance work that benefits from researchers who can operate with meaningful autonomy rather than requiring close day-to-day supervision.