Clinical Trial Manager
$120,000–$150,000 year
HybridBoston, Massachusetts, United States
Job Summary
Support day-to-day activities within oncology clinical trials, including country/site feasibility assessments, site selection, start-up, maintenance, and close-out. Serve as the key operational point of contact for CROs and trial sites, identifying and escalating potential issues. Assist with oversight of CRO and vendor set-up, liaising to ensure timely study initiation. Review site-level regulatory documents, escalate as needed, and help ensure inspection readiness, TMF quality, and adherence to protocol and regulatory requirements. Proactively identify operational challenges, propose mitigation plans, and monitor study performance metrics, timelines, and deliverables. Track study budgets and vendor invoices, maintain clinical operations trackers, and provide regular study updates to internal stakeholders. This hybrid role in Boston, MA requires 2-3 days onsite plus periodic travel. Salary is $120,000 - $150,000.
Required Qualifications
- Bachelor's degree in a scientific, healthcare, or related field, or an RN, required
- 3-4 years of Clinical Trial Manager or Clinical Project Management experience
- Legally authorized to work in the United States
Desired Qualifications
- ideally supporting oncology clinical trials
- Experience supporting oncology studies strongly preferred
- Vendor and CRO management experience
- Strong working knowledge of ICH-GCP guidelines and clinical trial regulations
- Excellent organizational, problem-solving, and time management skills
- Strong attention to detail
- Strong written and verbal communication skills
- collaborative, team-oriented approach
- Comfortable in a fast-paced, dynamic environment
- proactive, roll-up-your-sleeves mindset
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