Sr. Clinical Trial Associate
Rapport Therapeutics
Rapport Therapeutics seeks a Senior Clinical Trial Associate to support bipolar mania clinical studies in Boston. The role involves managing trial documentation, maintaining regulatory files, coordinating administrative tasks, and supporting the study team in a fast-paced biotech environment.
Responsibilities
- Coordinate distribution and retrieval of clinical documents including protocols, amendments, and monitoring reports
- Maintain inspection-ready Trial Master File according to ICH-GCP standards and company procedures
- Prepare study-related documents and track clinical trial equipment and supplies
- Support administrative aspects of contract execution, vendor invoicing, and clinical trial insurance updates
- Assist with meeting management, internal databases, study newsletters, and ad-hoc trial activities
Requirements
- Bachelor's degree in life sciences or healthcare-related field
- 3+ years clinical trial support experience; biotech or pharma background preferred
- Proficiency with Excel, Word, PowerPoint, and Outlook
- Understanding of clinical trial functions and regulatory requirements
- Ability to manage multiple priorities independently and maintain confidentiality
Vacancy posted more than 2 months ago
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