[Hiring] Senior Epidemiologist, Oncology, Breast Cancer, Real World Evidence - FSP @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.
• Lead development of study protocols, analysis plans, and study reports to answer research questions of priority to RWE.
• Lead, design, and manage epidemiological, biomarker and/or data science projects.
• Lead, plan, design, and conduct analyses for internal and external decision making.
• Lead the identification of fit-for-purpose data for the timely execution of the RWE strategy.
• Construct cohorts using RWD sources and evaluate key variables.
• Contribute to the communication of observational research results and methods.
• Support the effective communication of study/analysis results to support internal and external decisions.
• Coauthor abstracts and manuscripts for external dissemination of methodologic study results.
• Contribute to the development of processes and training aimed at increasing the efficiency, quality, and impact of functional activities.
Qualifications
• PhD in Epidemiology with a minimum of four (4) years of post-doctoral experience, preferably at a pharmaceutical company.
• Master’s degree in Epidemiology plus 7-9 years of experience in lieu of PhD may be acceptable.
• Oncology Specific: expert knowledge and extensive experience with cancer epidemiology.
• Pharmaco Epidemiology Specific: expert knowledge and extensive experience with pharmacoepi methods.
• 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, analysis, and interpretation is preferred.
• Demonstrated ability to function with an increasing level of autonomy.
• Ability to manage priorities and performance targets.
Requirements
• Ability to design studies independently.
• Extensive experience with oncology EMR databases.
• Extensive experience with conducting cancer epidemiology studies.
• Expert understanding of regulatory requirements for safety reporting and analysis.
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.
• Lead development of study protocols, analysis plans, and study reports to answer research questions of priority to RWE.
• Lead, design, and manage epidemiological, biomarker and/or data science projects.
• Lead, plan, design, and conduct analyses for internal and external decision making.
• Lead the identification of fit-for-purpose data for the timely execution of the RWE strategy.
• Construct cohorts using RWD sources and evaluate key variables.
• Contribute to the communication of observational research results and methods.
• Support the effective communication of study/analysis results to support internal and external decisions.
• Coauthor abstracts and manuscripts for external dissemination of methodologic study results.
• Contribute to the development of processes and training aimed at increasing the efficiency, quality, and impact of functional activities.
Qualifications
• PhD in Epidemiology with a minimum of four (4) years of post-doctoral experience, preferably at a pharmaceutical company.
• Master’s degree in Epidemiology plus 7-9 years of experience in lieu of PhD may be acceptable.
• Oncology Specific: expert knowledge and extensive experience with cancer epidemiology.
• Pharmaco Epidemiology Specific: expert knowledge and extensive experience with pharmacoepi methods.
• 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, analysis, and interpretation is preferred.
• Demonstrated ability to function with an increasing level of autonomy.
• Ability to manage priorities and performance targets.
Requirements
• Ability to design studies independently.
• Extensive experience with oncology EMR databases.
• Extensive experience with conducting cancer epidemiology studies.
• Expert understanding of regulatory requirements for safety reporting and analysis.
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