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Director- Real World Evidence (RWE) Oncology (Pharmacoepidemiology and Safety)
We are seeking a highly skilled Director to lead our Real-World Evidence (RWE) team in Oncology, focusing on pharmacoepidemiology and safety. The successful candidate will be responsible for designing and delivering RWE required by internal stakeholders and regulators, ensuring timeliness, quality, and utility.
Key Responsibilities:
- Design and deliver RWE studies for individual products and their pipeline/lifecycle indications in Oncology
- Provide functional perspective and subject-matter expertise on RWE methods and requirements at both the global/regional level and the TA level
- Collaborate and coordinate Pharmacovigilance and Safety projects within RWE Oncology Product teams
- Deliver post-authorization studies including patient registries, studies of natural history of disease, drug utilization studies, and more
Requirements:
- PhD, MD, ScD, PharmD) and/or Master's degree in Epidemiology or related discipline
- Minimum 8 years (PhD) or 10 years (MS) of relevant experience
- Direct experience with different applications of RWE, including early-stage clinical development, regulatory approvals, and/or safety commitments
About Us:
Gilead is a global biopharmaceutical company committed to creating a healthier world for all people. We're working tirelessly to develop therapies that help improve lives and ensure access to these therapies across the globe.
This position may also be eligible for a discretionary annual bonus, discretionary stock-based long-term incentives, paid time off, and a benefits package. Benefits include company-sponsored medical, dental, vision, and life insurance plans.