Top Tech Jobs & Startup Jobs in Boston, MA

The Director of Program Management oversees drug development assets, leads cross-functional teams, manages risks, and aligns on Target Product Profiles and Integrated Development Strategies, ensuring execution and resource advocacy.

The Senior Director, Program Management is responsible for leading high-priority drug development projects, executing integrated development strategies, managing teams, and ensuring alignment across sub-teams and governance levels.

The Senior Scientist will perform analytical characterization of large molecules, develop methods, maintain instrumentation, and manage contractor activities while collaborating with project teams.

The Scientific Associate Director - Toxicology oversees nonclinical safety evaluations, designs toxicity studies, collaborates with regulatory agencies, and develops safety strategies for drug candidates in various diseases.

The Scientist will analyze multi-dimensional biomarker data, conduct translational research using AI/ML methods, and collaborate with teams to drive drug development insights.

The Sr. Scientist will advance oncology drug discovery focusing on immunology and biotherapeutic target identification, utilizing wet lab work, to understand cancer biology and develop therapeutic approaches.

The Senior Clinical Trial Physician manages clinical trials, ensures medical accountability, collaborates with teams, and provides expert guidance in clinical development strategy.

The Senior Clinical Scientist leads and executes clinical trial activities, ensures adherence to protocols, collaborates with cross-functional teams, and supports clinical development planning while providing scientific and clinical leadership.

The Associate Director, Program Management will oversee cross-functional planning and execution for drug development projects, manage timelines, resource forecasts, and risk management while collaborating with multiple teams and leadership.

The Sr. Clinical Trial Physician oversees multiple clinical trials, providing medical accountability and expertise. Responsibilities include medical monitoring, clinical development strategy, health authority interactions, and authoring clinical documents based on extensive experience in the industry or academia.