
location_on577, Mallard Avenue, Durham, Durham County, North Carolina, 27701, United States
Join IQVIA's Sponsor-Dedicated FSP team, where we advance healthcare through real-world evidence (RWE). We bring together scientific expertise and real-world data to help sponsors make critical decisions and accelerate evidence generation to improve patient outcomes. Our platform group operates at the intersection of clinical research and commercial insights, creating intelligent connections to accelerate the development and commercialization of innovative medical treatments worldwide.
In this position, you will work closely with a single sponsor, gaining deep knowledge of their specific therapies while leveraging IQVIA's global expertise. You will serve as a strategic partner, operating with a high level of autonomy to design and conduct epidemiological studies that answer priority research questions. Your work will directly influence internal and external decision-making, ranging from responses to regulatory authorities to rapid analyses of safety queries.
You will lead the identification of fit-for-purpose data and construct cohorts using real-world data sources such as claims and electronic health records (EHR). Beyond execution, you will contribute to the communication of observational research results through regulatory documents, reports, publications, and white papers. This role is designed for a subject matter expert who can translate complex research questions into robust study designs and provide deep hands-on familiarity with EHR data curation behind health system firewalls.
This is your chance to make a tangible impact while building a career that matters. You will be part of a forward-thinking team that helps shape the next generation of evidence-based healthcare. By working hand-in-hand with a leading sponsor, you will gain deep expertise in their therapies and leverage IQVIA's global network to support your professional growth. Your contributions will help identify evidence gaps and develop options to address them, directly supporting clinical development programs.
To apply, please submit your resume and relevant credentials through the IQVIA careers portal. We appreciate your honesty and professionalism throughout the recruitment process. IQVIA is committed to integrity in our hiring process and maintains a zero-tolerance policy for candidate fraud. All information and credentials submitted must be truthful and complete; any false statements, misrepresentations, or material omissions will result in immediate disqualification or termination of employment.
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. We foster a culture of integrity and collaboration, inviting diverse perspectives to help us improve patient outcomes and population health worldwide.
Work model: Remote
577, Mallard Avenue, Durham, Durham County, North Carolina, 27701, United States
Durham, North Carolina
Experience in pharmaceutical industry, biotechnology, or consulting environment. A record of scientific publications demonstrating expertise in observational study design, analysis, and interpretation. Experience in leading drug development projects for 2+ years for the therapeutic area of assignment.
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Skills: Epidemiology, Biostatistics, Pharmacoepi Methods, Signal Detection, Validation Methods, Observational Research Methods, Study Design, Protocol Development, Statistical Analysis Plan, Study Report Development.
Education: PhD in Epidemiology, Biostatistics, Psychometrics, or related field required; Master's degree in epidemiology, biostatistics, bioinformatics, or relevant scientific field acceptable with 7-9 years experience.