Manager role at Pfizer overseeing clinical studies, focusing on project management, timelines, budget, and ensuring studies meet scope and quality parameters. Requires experience in pharmaceutical R&D and regulatory inspections.

This role involves managing various medical affairs projects at Pfizer, focusing on RMP (Risk Management Plan) deliverables and RWE (Real-World Evidence) projects. Responsibilities include consolidating and drafting RMP documentation for health authorities, coordinating RWE projects, managing study issues and compliance, tracking budget spending, and overseeing internal processes for medical projects like clinical research, non-interventional studies, and advisory boards. The role also involves budget planning, allocation, monitoring, and project closure.

This role involves monitoring drug surveillance programs, processing adverse reports for clinical trials and post-marketing activities, and ensuring compliance with regulatory requirements and corporate policies. The associate will analyze post-marketing safety data and determine appropriate workflows for case processing.