Epidemiologist, Virology, Real World Evidence (FSP Sponsor Dedicated)

Location: Remote, candidates must be US-based Join IQVIA’s Sponsor-Dedicated FSP team and help advance healthcare through real-world evidence. We bring together scientific expertise and real-world data to help sponsors make decisions and accelerate evidence generation to improve patient outcomes. In this role, you’ll work closely with one sponsor, gaining deep knowledge of their therapies while leveraging IQVIA’s global expertise. C ore F unct i o n D e s cr i pt i on : D e s ign an d c ondu ct e p i d em i o l o gic a l s t ud i e s to g e n e r a te r e a l-w o rld e v i d e n c e w it h in t i me , bud g e t, an d q u a lity s t and ar d s , i n cl ud i n g b u t n ot l i m it e d t o n at u r a l h i s t o ry o f d i s e as e , p o pu l a ti o n c h ar a ct e ri z a ti on , a s s e ss me n t o f tr e a t me n t p att e r n s an d un me t n ee d , d e v e l op me n t o f e x t e r na l c o m pa r a t o r s , b e n c h m a r k i n g o f cli n ic a l ou tc o me s , c o m pa r a ti v e sa fe t y an d eff e c t i v e n e s s r e s e a rc h , an d p o st - au t ho ri za ti o n s t u d i e s Requ i r ed E x p e r i enc e Developed and executed under Scientific Oversight study protocols, analysis plans, and study reports to answer research questions of priority to RWE. Designed and managed epidemiological, biomarker and/or data science projects. Planned, designed, and conducted analyses for internal and external decision making (e.g., responses to regulatory authorities, rapid analyses of safety queries). Supported the identification of fit-for-purpose data for the timely execution of the RWE strategy. Constructed cohorts using RWD sources (e.g., claims, EHR) and evaluate key variables, including diagnosis and procedures codes, and plan validation studies as needed. Conducted analyses for descriptive and comparative research using RWD (examples include claims, EHR, PRO/COA, registry data) for methodologic research questions. Contributed to the communication of observational research results and methods, including development of pertinent sections of regulatory documents, reports, publications, white papers. Supported the effective communication of study/analysis results to support internal and external decisions. Coauthored abstracts and manuscripts for external dissemination of methodologic study results. Contributed to the development of processes and training aimed at increasing the efficiency, quality, and impact of functional activities. Technical Expertise: Observational research methods (both Primary and Secondary Data Collection), deep knowledge of biostatistics and analysis methods, and understanding of regulatory processes. Project Implementation: Protocol writing, SAP, manuscript and abstract writing. Minimum Qualifications PhD in Epidemiology, Biostatistics, Psychometrics, 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, biostatistics, bioinformatics, or relevant scientific field, plus five (5) years of experience in lieu of PhD may be acceptable. 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. What’s in it for you? 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 who supports your growth. This is your chance to make an impact, while building a career that matters. 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 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. IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. The potential base pay range for this role, when annualized, is $109,200.00 - $273,000.00. 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 of compensation may be offered, in addition to a range of health and welfare and/or other benefits.