FSP Epidemiologist (Oncology) Position Available In Durham, North Carolina

FSP Epidemiologist (Oncology) FSP Epidemiologist (Oncology)
locations
Durham, North Carolina, United States of America
time type
Full time
posted on
Posted 2 Days Ago
job requisition id

R1466076

Location:

Remote, candidates must be US-based
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 externalparators, benchmarking of clinical oues,parative 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 andparative research using RWD for methodologic research questions
Contribute to themunication of observational research results and methods, including development of pertinent sections of regulatory documents, reports, publications, white papers.
Support the effectivemunication 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,mercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development andmercialization of innovative medical treatments to help improve patient oues and population health worldwide. 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. /eoe
The potential base pay range for this role, when annualized, is $135,000.00 – $225,000.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms ofpensation may be offered, in addition to a range of health and welfare and/or other benefits.