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Sr. Clinical Trial Associate

Rapport Therapeutics

Rapport Therapeutics seeks a Senior Clinical Trial Associate to support epilepsy clinical studies in Boston. The role involves managing trial documentation, maintaining regulatory files, coordinating vendor activities, and supporting study team operations.

Responsibilities

  • Coordinate distribution and retrieval of clinical trial documents and study materials
  • Maintain inspection-ready Trial Master File per ICH-GCP standards and company procedures
  • Prepare study-related documents including informed consent forms and clinical trial tools
  • Track vendor invoices, deliverables, timelines, and coordinate team communications
  • Support contract execution, purchase order generation, and administrative trial activities

Requirements

  • Bachelor's degree in life sciences or healthcare-related field
  • 3+ years clinical trial support experience in biotech, pharmaceutical, or CRO
  • Global clinical trial experience strongly preferred
  • Proficiency with Excel, Word, PowerPoint, and Outlook
  • Understanding of clinical trial functions and dependencies
  • Ability to manage multiple priorities independently in fast-paced setting
Vacancy posted 16 days ago
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