Search the 3 jobs at Pfizer

The Director of Study Management will oversee clinical studies in the Pfizer Biopharma Group, managing timelines, budgets, and resources to ensure compliance with strategic objectives. This role involves leading study teams, coordinating project deliverables, and establishing operational standards to enhance performance and drive innovation in patient care.

You will lead obesity clinical studies, manage timelines, budgets, and ensure studies are conducted within scope. Your role includes project management, resolving issues, collaborating with teams, and ensuring data flow and compliance as part of Pfizer's medical team.

The Oncology Medical Writer (Senior Manager/Associate Director) leads the development of regulatory documents related to clinical studies, ensuring compliance with internal and external standards. Responsibilities include managing document processes, collaborating with project teams, identifying information gaps, maintaining timelines, and proposing process improvements. The role requires effective communication and problem-solving skills to drive decision-making and document production.