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FSP Epidemiologist (Oncology)

IQVIA Argentina

Durham (NC)

On-site

USD 80,000 - 140,000

Full time

30+ days ago

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Job summary

An established industry player is seeking a skilled FSP Epidemiologist to design and conduct epidemiological studies in oncology. This role involves generating real-world evidence, supporting study protocol development, and conducting analyses using real-world data. The ideal candidate will have a PhD in Epidemiology or a related field, with a strong background in oncology research and observational methods. Join a leading global provider of clinical research services that is committed to improving patient outcomes and population health. If you are passionate about making a difference in healthcare, this opportunity is perfect for you.

Qualifications

  • PhD in Epidemiology or related field with relevant post-doctoral experience required.
  • Experience in oncology research and observational research methods is essential.

Responsibilities

  • Design and conduct epidemiological studies to generate real-world evidence.
  • Support development of study protocols, analysis plans, and reports.

Skills

Epidemiological Study Design
Oncology Research
Statistical Analysis
Data Analysis
Scientific Publications
Cross-functional Collaboration

Education

PhD in Epidemiology
Master's in Epidemiology or related field

Tools

Electronic Health Records (EHR)
Medical Claims Databases

Job description

FSP Epidemiologist, Oncology, Real World Evidence

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.
  • Support development of study protocols, analysis plans, and study reports to answer methodologic questions of priority to RWE.
  • Support 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.
  • Contribute to the communication of observational research results and methods, including development of pertinent sections of regulatory documents, reports, publications, and white papers.
  • Support the effective communication of study/analysis results to support internal and external decisions.
  • Contribute to the development of processes and training aimed at increasing the efficiency, quality, and impact of functional activities.
  • Coauthor abstracts and manuscripts for external dissemination of methodologic study results.

Minimum Requirements

  • PhD in Epidemiology or related field with a minimum of two (2) years of relevant post-doctoral experience, preferably in pharmaceutical industry, biotechnology, or consulting environment. Master’s degree in epidemiology or relevant scientific field, plus five (5) years of experience in lieu of PhD may be acceptable.
  • Experience in oncology research, specifically in solid tumors.
  • 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.
  • Knowledge of secondary data sources and experience with secondary data analysis, including electronic medical record and/or medical claims databases.
  • 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 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. Learn more at https://jobs.iqvia.com

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. https://jobs.iqvia.com/eoe

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