[Hiring] Senior Epidemiologist, Inflammation, IBD @IQVIA
Role Description
Join IQVIA’s Sponsor-Dedicated FSP team and help advance healthcare through real-world evidence. In this role, you’ll work closely with one sponsor, gaining deep knowledge of their therapies while leveraging IQVIA’s global expertise.
• Design and conduct epidemiological studies to generate real-world evidence within time, budget, and quality standards.
• Core functions include:
• 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
• Post-authorization studies
• Lead development of study protocols, analysis plans, and study reports.
• Lead, design, and manage epidemiological, biomarker and/or data science projects.
• Support internal and external decision making through analyses.
• Construct cohorts using RWD sources (e.g., claims, EHR).
• Contribute to communication of observational research results and methods.
• Coauthor abstracts and manuscripts for external dissemination.
• Contribute to the development of processes and training for efficiency and quality.
Qualifications
• PhD in Epidemiology, Biostatistics, Psychometrics, or related field with a minimum of four (4) years of relevant post-doctoral experience.
• Master’s degree in epidemiology, biostatistics, bioinformatics, or relevant scientific field, plus 7-9 years of experience in lieu of PhD may be acceptable.
• Deep understanding of observational research methods.
• Extensive knowledge of secondary data sources and experience with secondary data analysis.
• A record of scientific publications demonstrating expertise in observational study design.
• Demonstrated ability to function with increasing autonomy and develop cross-functional collaborations.
• Ability to manage priorities and performance targets.
• Experience in leading drug development projects for 2+ years preferred.
Requirements
• Ability to design studies independently.
• Deep, hands-on familiarity with EHR data curation.
• Expert knowledge and extensive experience with pharmacoepi methods.
• Leverage RWE expertise to identify evidence gaps.
Benefits
• 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.
Apply tot his job
Apply To this Job
Join IQVIA’s Sponsor-Dedicated FSP team and help advance healthcare through real-world evidence. In this role, you’ll work closely with one sponsor, gaining deep knowledge of their therapies while leveraging IQVIA’s global expertise.
• Design and conduct epidemiological studies to generate real-world evidence within time, budget, and quality standards.
• Core functions include:
• 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
• Post-authorization studies
• Lead development of study protocols, analysis plans, and study reports.
• Lead, design, and manage epidemiological, biomarker and/or data science projects.
• Support internal and external decision making through analyses.
• Construct cohorts using RWD sources (e.g., claims, EHR).
• Contribute to communication of observational research results and methods.
• Coauthor abstracts and manuscripts for external dissemination.
• Contribute to the development of processes and training for efficiency and quality.
Qualifications
• PhD in Epidemiology, Biostatistics, Psychometrics, or related field with a minimum of four (4) years of relevant post-doctoral experience.
• Master’s degree in epidemiology, biostatistics, bioinformatics, or relevant scientific field, plus 7-9 years of experience in lieu of PhD may be acceptable.
• Deep understanding of observational research methods.
• Extensive knowledge of secondary data sources and experience with secondary data analysis.
• A record of scientific publications demonstrating expertise in observational study design.
• Demonstrated ability to function with increasing autonomy and develop cross-functional collaborations.
• Ability to manage priorities and performance targets.
• Experience in leading drug development projects for 2+ years preferred.
Requirements
• Ability to design studies independently.
• Deep, hands-on familiarity with EHR data curation.
• Expert knowledge and extensive experience with pharmacoepi methods.
• Leverage RWE expertise to identify evidence gaps.
Benefits
• 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.
Apply tot his job
Apply To this Job