IQVIA
Location: Remote, candidates must be US-based
Overview Responsibilities
Design and conduct epidemiological studies to generate real-world evidence within time, budget, and quality standards, including natural history of disease, population characterization, assessment of treatment patterns and unmet need, development of external comparators, benchmarking of clinical outcomes, comparative safety and effectiveness research, and post-authorization studies.
Lead development of study protocols, analysis plans, and study reports to answer methodologic questions of priority to real-world evidence (RWE).
Lead the identification of fit-for-purpose data for the timely execution of the RWE strategy.
Construct cohorts using real-world data sources (e.g., claims, EHR) and evaluate key variables, including diagnosis and procedures codes; plan validation studies as needed.
Conduct analyses for descriptive and comparative research using real-world data for methodologic research questions.
Lead the communication of observational research results and methods, including development of pertinent sections of regulatory documents, reports, publications, and white papers.
Lead effective communication of study/analysis results to support internal and external decisions.
Coauthor abstracts and manuscripts for external dissemination of methodologic study results.
Demonstrate the ability to manage stakeholders including external vendors and internal cross-functional teams.
Bring strong epidemiologic methodologic expertise, a track record of designing innovative RWE studies, and the ability to translate complex data into actionable insights for internal and external stakeholders.
Minimum Requirements
PhD in Epidemiology or related field with a minimum of four (4) years of relevant post-doctoral experience; or Master’s degree in epidemiology or relevant field with seven (7) years of experience in lieu of PhD.
Understanding of observational research methods and experience to support the design and conduct of observational research, including protocol, statistical analysis plan, and study report development.
Extensive experience in both secondary database studies and primary data collection, including electronic medical record and/or medical claims databases.
Experience working with commercially available US datasets and data platforms.
Preferred experience in chronic autoimmune inflammatory conditions such as rheumatoid arthritis, atopic dermatitis, lupus, and asthma.
Experience in innovative study designs, such as synthetic control arms, external comparators, and hybrid real-world data–clinical trial approaches, to support clinical development and regulatory decision-making.
A record of scientific publications demonstrating expertise in observational study design, analysis, and interpretation.
Demonstrated ability to function with increasing autonomy and to develop productive cross-functional collaborations in a matrix environment.
Ability to manage priorities and performance targets.
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
The potential base pay range for this role, when annualized, is $110,500.00 - $276,100.00. 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.
Seniority level
Not Applicable
Employment type
Full-time
Job function
Research, Analyst, and Information Technology
Industries
Pharmaceutical Manufacturing
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Overview Responsibilities
Design and conduct epidemiological studies to generate real-world evidence within time, budget, and quality standards, including natural history of disease, population characterization, assessment of treatment patterns and unmet need, development of external comparators, benchmarking of clinical outcomes, comparative safety and effectiveness research, and post-authorization studies.
Lead development of study protocols, analysis plans, and study reports to answer methodologic questions of priority to real-world evidence (RWE).
Lead the identification of fit-for-purpose data for the timely execution of the RWE strategy.
Construct cohorts using real-world data sources (e.g., claims, EHR) and evaluate key variables, including diagnosis and procedures codes; plan validation studies as needed.
Conduct analyses for descriptive and comparative research using real-world data for methodologic research questions.
Lead the communication of observational research results and methods, including development of pertinent sections of regulatory documents, reports, publications, and white papers.
Lead effective communication of study/analysis results to support internal and external decisions.
Coauthor abstracts and manuscripts for external dissemination of methodologic study results.
Demonstrate the ability to manage stakeholders including external vendors and internal cross-functional teams.
Bring strong epidemiologic methodologic expertise, a track record of designing innovative RWE studies, and the ability to translate complex data into actionable insights for internal and external stakeholders.
Minimum Requirements
PhD in Epidemiology or related field with a minimum of four (4) years of relevant post-doctoral experience; or Master’s degree in epidemiology or relevant field with seven (7) years of experience in lieu of PhD.
Understanding of observational research methods and experience to support the design and conduct of observational research, including protocol, statistical analysis plan, and study report development.
Extensive experience in both secondary database studies and primary data collection, including electronic medical record and/or medical claims databases.
Experience working with commercially available US datasets and data platforms.
Preferred experience in chronic autoimmune inflammatory conditions such as rheumatoid arthritis, atopic dermatitis, lupus, and asthma.
Experience in innovative study designs, such as synthetic control arms, external comparators, and hybrid real-world data–clinical trial approaches, to support clinical development and regulatory decision-making.
A record of scientific publications demonstrating expertise in observational study design, analysis, and interpretation.
Demonstrated ability to function with increasing autonomy and to develop productive cross-functional collaborations in a matrix environment.
Ability to manage priorities and performance targets.
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
The potential base pay range for this role, when annualized, is $110,500.00 - $276,100.00. 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.
Seniority level
Not Applicable
Employment type
Full-time
Job function
Research, Analyst, and Information Technology
Industries
Pharmaceutical Manufacturing
Referrals increase your chances of interviewing at IQVIA by 2x
Get notified about new Senior Epidemiologist jobs in Minneapolis, MN.
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