Clinical Study Administrator - Contracts And Budgets

medizinstellenmarkt.de

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.
  • Serve as primary point of contact for legal negotiations related to confidentiality agreements and amendments.
  • Ensure compliance with AstraZeneca’s Code of Ethics, policies and procedures, including those related to people, finance, technology, security and Safety, Health and Environment (SHE).

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)
  • ICH-GCP and local regulations knowledge

Nice-to-have

  • Personal effectiveness and self-accountability
  • Learning agility
  • Financial, technology and process competency
  • Cultural awareness
  • Efficient delivery of quality clinical trials

Key Requirements

  • Bachelors degree aligned to the knowledge and skills required
  • 0+ years of experience
  • Relevant knowledge of drug development process
  • Fluency in written and spoken business-level English
  • Ability to travel nationally and internationally

Work Rights

Not specified

Tailored Resume

Cover Letter