Top Operations Jobs

The Strategic Insights Associate will support Pfizer's Global Supply teams by creating and maintaining procurement analytics reports, managing data quality, and assisting in market intelligence and sourcing strategies. The role involves collaboration with cross-functional teams to drive data-driven decision-making and development of sourcing analytics.

The Strategic Insights Partner supports Pfizer's Global Supply sourcing teams by executing procurement analytics requests, creating reports, and maintaining a market intelligence repository. Responsibilities include delivering insights for budgeting, supplier negotiations, and understanding sourcing opportunities, as well as ensuring data accuracy and working within cross-functional teams to build data-driven strategies.

As an ES Supply Chain Specialist at Pfizer, you will oversee supply chain management activities for multiple contract manufacturers globally. Your responsibilities include managing document flows, ensuring timely transactions, coordinating shipments, and supporting project milestones. You will also analyze supply chain data and collaborate with team members to improve processes and performance, contributing directly to operational excellence in delivering medicines to patients.

The ISE India Lead is responsible for delivering strategic analytics and insights to support Pfizer's commercial strategy. This role involves leading cross-functional teams to solve complex business issues, drive performance measurement, engagement with business leaders, and development of analytic solutions. The lead acts as a strategic advisor to senior leadership and ensures team collaboration to meet business objectives.

The Late-Stage Clinical Scientist is responsible for the scientific oversight and quality of clinical trials in the Late-Stage Oncology portfolio. They lead and collaborate with various teams, author key documents, analyze safety data, and manage clinical scientists and contingent workers. The role requires extensive clinical research experience and knowledge in oncology and regulatory affairs.

Responsible for managing scientific oversight and data integrity of late-stage oncology clinical trials. Collaborates with clinical and medical teams, authors clinical documentation, analyzes data for safety profiles, and leads data review strategies. The candidate may supervise Clinical Scientists and contribute to process improvements in clinical development.

The Director, Medical Monitor is responsible for overseeing clinical trials, ensuring patient safety, providing medical expertise, and designing development strategies for regulatory approval. They monitor safety data, assist with protocol design, provide clinical input, and support study teams to maintain data integrity.