Senior Clinical Trial Manager
$153,000–$197,600 year
On-siteWatertown, Massachusetts, United States
Job Summary
Manage clinical CROs and vendors from initial contact through final deliverables, ensuring study conduct aligns with ICH/GCP, federal regulations, and internal SOPs. Lead external trial management teams to coordinate clinical monitoring, data management, medical writing, and safety activities. Prepare study materials, track enrollment, and develop timelines while proactively identifying risks and implementing mitigation strategies. Support the management and maintenance of the Trial Master File held by the CRO. Attend site visits, including pre-study selection and PI engagement meetings, to oversee operational execution. This role reports to the VP, Clinical Operations within Treeline Biosciences' growing Clinical Development group.
Required Qualifications
- Bachelor's degree, or equivalent, in a biomedical, life science or related field of study
- 5-8+ years of trial management experience as primary Clinical Trial Manager (or equivalent) within Pharma, Biotech or CRO
- Oncology experience
- Strong understanding of global regulatory and compliance requirements for clinical research
- Strategic understanding of how outcomes, budgets, and timelines are impacted by decisions
- Outstanding teamwork, organizational, interpersonal, and problem-solving skills
- Effective communicator both verbally and in written form
- Ability to influence and collaborate well with colleagues and partners in a fast-paced growing development company
- This role is based out of our Watertown, MA office and is not a remote role
- This position is classified as exempt
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