Top Operations Jobs

As a Senior Associate in External Supply, you will ensure timely drug product delivery and maintain quality compliance by collaborating with vendors and project teams. Responsibilities include handling RFQs, supporting GMP activities, overseeing outsourcing programs, and managing the supply chain process, ensuring accurate reporting and financial oversight.

The Medical Scientific Liaison (MSL) is responsible for scientific discussions around Pfizer's products, ensuring compliance and integrity in communications, and supporting external healthcare professionals (HCPs) through accurate scientific data dissemination. This role requires collaboration with internal teams and engagement with external stakeholders to maintain strategic partnerships and contribute to medical strategies.

The CT Platform Safety Associate is responsible for reviewing and processing clinical study and adverse event reports to ensure the safety profile of Pfizer's products. This role includes data entry, case assessment, documentation, compliance verification, and collaboration with various stakeholders.

The Director for HTA, Value & Evidence will drive optimal patient access for Pfizer's breast cancer medicines, particularly Atirmociclib, by developing and executing global evidence generation strategies. Responsibilities include leading health economics research, coordinating evidence needs across teams, designing global HEOR studies, and developing strategic partnerships to support market access and reimbursement efforts.

The Director of HTA, Value & Evidence for Breast Cancer will lead the evidence generation strategy for Atirmociclib, managing HEOR activities to support global patient access and reimbursement strategies. Responsibilities include coordinating input on evidence needs, executing global HEOR studies, developing launch deliverables, and creating partnerships with external experts and stakeholders.

The Late-Stage Clinical Scientist (Manager) oversees scientific integrity and quality in oncology clinical trials. Responsibilities include supporting clinical operations, authoring regulatory documents, analyzing clinical data, and ensuring compliance with SOPs and regulations. The role involves collaboration with clinical and safety colleagues to assess drug safety profiles and contribute to the optimization of clinical procedures.

The Late-Stage Clinical Scientist (Manager) will oversee the scientific integrity and quality of oncology clinical trials. Responsibilities include supporting clinical development, authoring key documents, analyzing safety data, and improving clinical procedures. Requires collaboration with other professionals and compliance with regulations.