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[Hiring] Epidemiologist, Oncology, Real World Evidence @IQVIA

Work from home Full-time role Hiring

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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