Sr. Clinical Trial Associate

Triveni Bio

Watertown, MA, United States
On-site
Ich-gcp knowledge
Trial master file (tmf) maintenance
Ctms usage
Triveni Bio is seeking a Sr. Clinical Trial Associate to support the planning and execution of clinical trials, ensuring compliance with regulatory standards. The ideal candidate should have a background in life sciences, at least two years of CTA experience, and proficiency in clinical trial management tools

Job Summary

  • The Sr. Clinical Trial Associate supports the planning, execution, and oversight of clinical trials from study start-up through close-out.
  • This individual plays a critical role in maintaining study documentation, tracking operational activities, and ensuring compliance with ICH-GCP, regulatory requirements, and internal SOPs.
  • The Sr. CTA collaborates cross-functionally with internal teams, CROs, and clinical sites to ensure high-quality trial conduct.

Matching Summary

Match Score: 85

Triveni Bio is seeking a Sr. Clinical Trial Associate to support the planning and execution of clinical trials, ensuring compliance with regulatory standards. The ideal candidate should have a background in life sciences, at least two years of CTA experience, and proficiency in clinical trial management tools.

Skills & Requirements

Must-have

  • ICH-GCP knowledge
  • Trial Master File (TMF) maintenance
  • CTMS usage
  • CRO and vendor collaboration
  • Study document preparation
  • Site activation tracking

Nice-to-have

  • Patient impact focus
  • Bold and rigorous science
  • Open collaboration
  • Kindness and respect
  • Global experience a plus

Key Requirements

  • Bachelor's degree in life sciences
  • 2 years CTA experience
  • Experience with eTMF systems
  • Experience with CTMS
  • Ability to work on-site

Work Rights

Not specified

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