Clinical Study Administrator - Contracts And Budgets

Trzdev7

Study coordination and administration
Document management and submissions
Contracts, payments and legal interactions
Assist the Local Study Team with the coordination and administration of clinical studies from start‑up through execution and close‑out

Job Summary

  • Assist the Local Study Team with the coordination and administration of clinical studies from start‑up through execution and close‑out.
  • Take operational responsibility for correct set‑up and ongoing maintenance of the local electronic Trial Master File (eTMF) and Investigator Study File (ISF).
  • Serve as primary point of contact for legal negotiations related to confidentiality agreements and amendments.

Matching Summary

Assist the Local Study Team with the coordination and administration of clinical studies from start‑up through execution and close‑out.

Skills & Requirements

Must-have

  • Study coordination and administration
  • Document management and submissions
  • Contracts, payments and legal interactions
  • Clinical study operations (GCP)
  • Good Documentation Practice (GDP)

Nice-to-have

  • Personal effectiveness and strong self-accountability
  • Learning agility
  • Financial, technology and process competency
  • Ability to identify and champion more efficient delivery

Key Requirements

  • Bachelors degree aligned to the knowledge and skills required
  • 0+ experience required
  • Relevant knowledge of drug development process
  • International guidelines (ICH-GCP)
  • Applicable country regulations

Work Rights

Not specified

Tailored Resume

Cover Letter