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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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