[Hiring] Epidemiologist, Oncology, Real World Evidence @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. Overview:

• Design and conduct epidemiological studies to generate real-world evidence within time, budget, and quality standards.
• Focus areas 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
• Operate strategically under limited supervision with a deep understanding of current Epidemiology research methods.

Responsibilities:

• Develop study protocols, analysis plans, and study reports to answer research questions of priority to RWE.
• Design and manage epidemiological, biomarker and/or data science projects.
• Lead, plan, design, and conduct analyses for internal and external decision making.
• Identify fit-for-purpose data for the timely execution of the RWE strategy.
• Construct cohorts using RWD sources and evaluate key variables.
• Communicate observational research results and methods.
• Support effective communication of study/analysis results.
• Coauthor abstracts and manuscripts for external dissemination.
• Contribute to the development of processes and training for efficiency and quality.

Technical Expertise:

• Observational research methods (both Primary and Secondary).
• Deep knowledge of biostatistics and analysis methods.
• Understanding of regulatory processes.
• Ability to design studies independently.

Subject Matter Expertise:

• Conduct analyses for descriptive and comparative research using RWD.
• Lead design and execution of post-marketing and observational safety studies.
• Engage with regulatory authorities to provide scientific input and ensure compliance.

Qualifications

• PhD in Epidemiology with a minimum of 2 years of post-doctoral experience, preferably at a pharmaceutical company.
• Master’s degree in Epidemiology plus 5-7 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.
• Demonstrated ability to function with increasing autonomy and develop cross-functional collaborations.
• Ability to manage priorities and performance targets.

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 that supports your growth.
• This is your chance to make an impact while building a career that matters.

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