Position Overview
- Senior Project Manager providing cross-functional project management and operational leadership with the Clinical Operations Team.
- Hybrid (Boston office): three in-office days each week.
Responsibilities
- Drive Clinical Operations core work: create integrated project plans; track milestones/metrics; monitor budgets, invoices, and accruals.
- Provide cross-functional transparency on clinical trial progress, including CRO/partner deliverables.
- Organize internal/external meetings (agendas, minutes, presentations).
- Manage ancillary supplies for clinical trials.
- Support risk management (risk assessment, mitigation planning) and audit preparation/follow-up.
- Contribute to clinical study plans/manuals (version tracking, team training).
- Support senior leadership defining trial deliverables aligned to departmental/company goals.
- Maintain ongoing stakeholder communication (senior leadership and external partners/vendors).
- Foster inclusion and shared purpose.
Qualifications
- Bachelorβs degree in life sciences or related field (required).
- 5+ years biotech/pharma industry experience; 3+ years project management in biotech/pharma (preferred: oncology clinical trials; knowledge of ICH/GCP and related guidelines).
- Strong project planning/execution/tracking and risk identification/management experience.
- Strong organizational/leadership, analytical/problem-solving, and communication skills.
- Ability to prioritize and manage multiple cross-functional tasks in a fast-paced environment.
- Travel: up to 10β15%.