Top Biotech Project Management Jobs in Boston, MA

Manage TMF documentation transitions within Novartis for M&A and licensing projects, ensuring compliance and process improvement in clinical document management.

The Director, CQA/GCP Auditing Lead oversees GCP audits, ensuring compliance across clinical studies. Responsibilities include planning audits, writing reports, tracking metrics, and supporting inspection readiness.

The Director of Global Regulatory Project Management leads oncology regulatory strategies, ensures timely submissions, manages global project teams, and fosters cross-regional collaboration to maintain market access for products.

Oversee Quality Control data tracking and reporting, collaborate with QC teams, maintain tracking systems, ensure compliance, and coordinate QC activities.

The Biopharma Project Manager oversees project coordination and communication for antibody discovery projects, ensuring customer satisfaction throughout the process.

The Director of R&D Learning Business Partner leads a team to design and implement strategic learning initiatives, driving performance and innovation aligned with business priorities in R&D.

Manage and optimize planning, execution, and tracking for biotech development initiatives, utilizing Smartsheet and other PM tools for effective project management.

The Project Management Specialist coordinates equipment implementation, manages project schedules, liaises with customers, and focuses on successful project execution.

The Associate Director of TMF oversees Trial Master File operations, ensuring compliance and inspection readiness, while leading a team and collaborating cross-functionally.

The Manager of Quality Management Systems oversees compliance with regulations, manages quality documentation, promotes continuous improvement, and ensures inspections readiness in partnership with cross-functional teams.