Our client, a biopharmaceutical company based in Boston, is seeking a Clinical Trials Project Manager to oversee the execution of Phase II and Phase III clinical studies. This role manages timelines, budgets, and vendor relationships across multiple concurrent trials while ensuring compliance with FDA regulations and Good Clinical Practice standards.
The position works closely with clinical operations, regulatory affairs, biostatistics, and external contract research organizations to keep studies on track. The ideal candidate has direct experience managing trial milestones, site selection, and data quality oversight in a regulated pharmaceutical or biotech environment.
This is a hybrid contract role based in Boston, with on-site presence required for study team meetings, site initiation visits, and sponsor audits. The engagement is expected to run through the end of the study's current phase, with potential for extension based on program needs.
| Location | Boston, MA |
| Job Type | Contractor |
| Salary | $95,000–$125,000 Per Year |
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