IQVIA
4 days ago Be among the first 25 applicants
Location : Remote, candidates must be US-based
Description :
Design and conduct epidemiological studies to generate real-world evidence within time, budget, and quality standards, including but not limited to 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 RWE
Lead the identification of fit‑for‑purpose data for the timely execution of the RWE strategy
Construct cohorts using RWD sources (e.g., claims, EHR) and evaluate key variables, including diagnosis and procedures codes, and plan validation studies as needed
Conduct analyses for descriptive and comparative research using RWD for methodologic research questions
Lead the communication of observational research results and methods, including development of pertinent sections of regulatory documents, reports, publications, 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
Demonstrated ability to manage stakeholders including external vendors and internal cross‑functional teams
The ideal candidate will 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, preferably in pharmaceutical industry, biotechnology, or consulting environment. Master’s degree in epidemiology or relevant scientific field, plus seven (7) years of experience in lieu of PhD may be acceptable.
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 background 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 RWD‑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 an increasing level of 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.
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.
Job pay range approximate: $110,500.00 - $276,100.00 annually.
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Location : Remote, candidates must be US-based
Description :
Design and conduct epidemiological studies to generate real-world evidence within time, budget, and quality standards, including but not limited to 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 RWE
Lead the identification of fit‑for‑purpose data for the timely execution of the RWE strategy
Construct cohorts using RWD sources (e.g., claims, EHR) and evaluate key variables, including diagnosis and procedures codes, and plan validation studies as needed
Conduct analyses for descriptive and comparative research using RWD for methodologic research questions
Lead the communication of observational research results and methods, including development of pertinent sections of regulatory documents, reports, publications, 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
Demonstrated ability to manage stakeholders including external vendors and internal cross‑functional teams
The ideal candidate will 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, preferably in pharmaceutical industry, biotechnology, or consulting environment. Master’s degree in epidemiology or relevant scientific field, plus seven (7) years of experience in lieu of PhD may be acceptable.
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 background 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 RWD‑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 an increasing level of 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.
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.
Job pay range approximate: $110,500.00 - $276,100.00 annually.
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