Sr. Clinical Trial Manager
Sr. Clinical Trial Manager
Location: Waltham, MA (Hybrid on-site 3x weekly) Therapeutic Area: Rare Disease Job Overview: You will manage internal and external teams, oversee CROs and vendors, and ensure trials are conducted in compliance with regulatory standards and timelines. Primary Job Responsibilities:- Serve as primary operational contact for assigned clinical trials
- Lead weekly Clinical Trial Team meetings and manage study timelines
- Oversee CROs, vendors, and site-facing activities including PI meetings and site visits
- Support development of study documents (protocols, ICFs, CRFs, etc.)
- Maintain and oversee Trial Master File (TMF) for inspection readiness
- Identify and mitigate risks proactively across study execution
- Coordinate training for study teams, sites, and vendors
- Ensure compliance with ICH-GCP, regulatory guidelines, and internal SOPs
- Contribute to vendor selection and oversight
- Collaborate cross-functionally to resolve trial issues and implement corrective actions
Primary Job Requirements:
- 5+ years of Clinical Operations experience in biotech, pharma, or CRO
- Proven track record managing multiple clinical trials
- Strong understanding of US regulatory and GCP requirements
- Bachelor's degree in life sciences or related field
- Excellent communication, leadership, and problem-solving skills
- Proficient in Microsoft Office and clinical trial systems
- Willingness to travel up to 25%
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