Associate Director of ; Pharma Co - Remote

Position

Associate Director of Real World Evidence (Pharma Co Experience Required) – Remote US

• This role is open to US employees with no sponsorship needs
• Skillset: AD Epi Pharma Co Epi, writing protocols, working with analysts, troubleshooting code lists, CPRD
• Pharma Co experience required

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 evaluated key variables, including diagnosis and procedures codes, and planned validation studies as needed
• Conducted analyses for descriptive and comparative research using RWD (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

Observational research methods (both primary and secondary data collection), deep knowledge of biostatistics and analysis methods, understanding of regulatory processes.

Protocol writing, SAP, manuscript and abstract writing.

Benefits for this position may include a company car or car allowance, health benefits (medical, dental, vision), company match 401(k), eligibility to participate in Employee Stock Purchase Plan, eligibility to earn commissions/bonus based on company and individual performance, and flexible paid time off (PTO) and sick time. Eligibility may vary based on state regulations.

$ – $.

Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The company may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered. The company will determine what constitutes as equivalent to the qualifications described above. No contractual obligations are created by this description. The company complies with the Americans with Disabilities Act, providing reasonable accommodations.

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 clinical outcomes, comparative safety and effectiveness research, and post‑authorization studies.