Jobs at Pfizer

Lead CBx business operations including finance, contracting, vendor lifecycle management, quality/document systems, audits, and data/QC. Drive process improvements, manage vendor contracts and PO/invoice coordination, maintain documentation systems, produce CBx metrics, and support cross-functional compliance and operational initiatives.

The Oncology Clinical Development Scientist will oversee clinical trials, ensuring data integrity and quality while collaborating with clinical teams to achieve successful outcomes in oncology research.

The Medical Director leads late-phase clinical trials in Hematology, ensuring compliance with standards and guiding the clinical operations team while collaborating with various departments and stakeholders.

As an AI Data Engineer, you will develop full stack applications integrating AI capabilities to support pharmaceutical research, enhancing workflows and productivity. Responsibilities include collaborating with researchers, developing scalable backend services, and deploying systems in AWS.

The Global Development Lead manages clinical development for assigned assets in Internal Medicine, leading cross-functional teams and ensuring regulatory compliance and study execution.

The Global Development Lead oversees clinical development for Internal Medicine assets, leading cross-functional teams in study design, execution, regulatory submissions, and providing expertise in chronic weight management and endocrinology.

Develop, validate, and interpret ML models and end-to-end pipelines to predict oral drug absorption using large, heterogeneous biopharmaceutics and clinical datasets. Emphasize model explainability, uncertainty quantification, and mechanistic/physics-informed approaches, translate outputs into actionable insights for drug development teams, and communicate results via reports, presentations, and publications while contributing to AI-enabled predictive platforms.

Lead translational biomarker strategy and execution for inflammatory and autoimmune assets across development phases. Provide scientific and technical leadership for assay development, validation, CRO management, protocol and regulatory contributions, data interpretation, and cross-functional collaboration to deliver regulatory-compliant biomarker data supporting program decisions and submissions.

The Senior Medical Director oversees clinical development in breast oncology, leads clinical trials, manages regulatory interactions, and provides strategic guidance. This role requires substantial experience in cancer trials and expertise in medical monitoring.

Responsible for scientific oversight of clinical trials in Late-Stage Oncology, partnering with teams for successful execution, and authoring essential documents. Expertise required in regulatory processes and clinical research theory, with significant prior experience.

Lead clinical development strategy and execution for GI oncology programs; design and oversee trials, safety and dose decisions, regulatory interactions, and cross-functional leadership. Serve as external clinical expert and manage medical directors and study teams.

Proactively source and engage AI and digital talent for the CMO AI Acceleration team, build and maintain pipelines, support screening and interview coordination, manage candidate data in ATS, and provide market intelligence to hiring partners.

The Senior Medical Director will lead clinical trials and support development strategies in hematology, ensuring compliance and safety while communicating complex concepts effectively.

Build and scale an AI-ready data architecture for biologics labs: develop data products, integration pipelines, agentic AI/LLM-enabled analysis, validate methods, improve metadata and storage, collaborate externally, onboard colleagues, and publish scientific work.

Provide clinical development leadership for the atirmociclib breast oncology program, including medical monitoring, investigator interactions, regulatory document development, cross-functional collaboration, strategic guidance, data interpretation, and representation in external engagements. Serve as Clinical Development Lead on study subteams and support marketing authorization activities while ensuring scientific, ethical, and regulatory compliance.

Senior enterprise executive to define and lead Pfizer's global obesity strategy, owning portfolio, capital allocation, cross‑functional alignment, and external representation. Drives enterprise decision‑making, scientific and commercial integration, and executive governance across R&D, Commercial, Medical, Development, and Finance in a global matrix.

The role involves designing and deploying AI systems for clinical operations, developing models for decision-making, and ensuring AI implementation aligns with data governance standards. Responsibilities include collaborating across teams, enhancing operational efficiency, and advancing AI applications in a regulated environment.

Responsible for data oversight and analysis in Oncology, managing team members and ensuring quality and integrity of clinical data for late-stage studies.

The Global Development Lead oversees clinical development for Internal Medicine assets, leading cross-functional teams, ensuring regulatory submissions, and providing input on clinical strategies in line with global standards.

The Clinical Development Scientist, Director will lead complex clinical trials in Inflammation and Immunology, ensuring scientific quality and patient safety. Responsibilities include protocol development, data interpretation, and implementing AI solutions in clinical workflows.