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The Quality Assurance Associate will manage GMP records, support regulatory audits, execute established procedures, and participate in continuous improvement activities within Document Control.

Lead and coordinate early oncology clinical studies, ensuring scientific leadership, protocol development, data analysis, and collaboration with cross-functional teams to meet trial objectives.

The Senior Medical Director will oversee clinical trial leadership, monitor medical activities, and collaborate on development strategies for hematology programs.

The Associate Director, Biostatistics is responsible for statistical guidance in clinical study design, data analysis, and regulatory submissions, leading clinical study teams to ensure timely and quality outcomes.

The Director, Oncology Early-Stage Clinical Scientist leads clinical research studies in oncology, focusing on the scientific execution and strategic planning of early clinical development for novel drugs.

Responsible for scientific oversight and quality of late-stage oncology clinical trials, partnering with colleagues to ensure successful execution, protocol authoring, and data analysis.

The role involves oversight of clinical trials in Late-Stage Oncology, ensuring data integrity, collaborating with teams, and authorship of key clinical documents.

The Quality Control Analyst II conducts routine and non-routine testing, manages lab equipment, and ensures GMP compliance in lab activities. Responsibilities include sample testing, environmental monitoring, and SOP creation for quality assurance processes.

The Senior Oncology Account Specialist promotes Pfizer's products to healthcare providers, enhances patient care, and builds strong relationships within healthcare environments.

The Regulatory Data Steward manages master data crucial for regulatory compliance, collaborates with cross-functional teams, and supports data governance strategies.