Clinical Trial Associate

Summittherapeutics

Palo Alto, California, USA
**
Clinical operations workflow support
Administrative support to study teams
Etmf oversight
** Summit Therapeutics is seeking a Clinical Trial Associate to support clinical operations in their oncology-focused studies. The ideal candidate will provide administrative support, manage documentation, and coordinate activities across study teams, all while adhering to regulatory standards. **

Job Summary

  • The Clinical Trial Associate (CTA) is responsible for supporting the daily workflow of clinical operations activities and providing administrative support to study teams throughout the study.
  • Key administrative activities include managing meeting invitations, creating agendas and meeting minutes, study document filing, maintaining study trackers, and oversight of the eTMF and vendors.
  • Ensures accurate and timely documentation, including eTMF management, study contracts and financial records in compliance with ICH-GCP, company policies and regulatory requirements.

Matching Summary

Match Score: 75

** Summit Therapeutics is seeking a Clinical Trial Associate to support clinical operations in their oncology-focused studies. The ideal candidate will provide administrative support, manage documentation, and coordinate activities across study teams, all while adhering to regulatory standards. **

Skills & Requirements

Must-have

  • Clinical operations workflow support
  • Administrative support to study teams
  • eTMF oversight
  • Vendor oversight
  • Study document filing
  • Maintaining study trackers

Nice-to-have

  • Passion for excellence
  • Purposeful urgency
  • Collaboration
  • Commitment to people

Key Requirements

  • ICH-GCP compliance

Work Rights

Not specified

Tailored Resume

Cover Letter