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Responsible for scientific oversight and quality of clinical trials in Late-Stage Oncology, collaborating with teams and presenting data, while ensuring compliance and optimizing procedures.

The Senior Manager, Portfolio Sourcing will lead sourcing efforts, manage vendor relationships, negotiate contracts, and ensure alignment with Pfizer's R&D portfolio strategies.

The Global Development Lead manages clinical development for assigned assets, leads cross-functional teams, oversees regulatory submissions, and provides expertise in therapeutic areas. Responsibilities include developing clinical plans, partnering with trial clinicians, and ensuring compliance with regulations.

The Medical Director will lead clinical trial support, ensure medical monitoring, collaborate on data interpretation, and guide teams while maintaining high expertise in oncology.

The role involves designing and delivering cloud-based HPC solutions, managing infrastructure automation, and ensuring operational excellence in scientific computing.

The Group Lead manages data cleaning and reporting processes, oversees teams, ensures high-quality analytics delivery, and drives operational excellence in clinical data analysis.

This role leads early oncology clinical studies development, coordinates with teams, ensures quality clinical trial execution, and interprets clinical data.

The Global Development Lead oversees clinical development for Internal Medicine, managing cross-functional teams and leading regulatory submissions, clinical trials, and external collaborations.

The Senior Medical Director leads clinical development in oncology, supporting clinical trials, managing teams, and ensuring compliance with scientific and regulatory standards.

The Quality Assurance Associate ensures compliance with GMP by processing records, supporting audits, and improving document control related to GMP records.