Clinical Study Contracts Coordinator

7 days ago


Durham, North Carolina, United States IQVIA Full time
Job Description:

As a Clinical Study Contracts Coordinator at IQVIA, you will play a crucial role in the preparation and execution of clinical study contracts in close collaboration with the SSO Study Start-Up Managers and the SSO Finance Specialists. Your primary responsibility will be to ensure compliance with GCP/ICH and regulatory requirements.

Key Responsibilities:
  • Support the country SSU strategy to ensure SSU timelines and deliverables are met according to country commitments.
  • Coordinate, prepare and execute clinical study contracts and amendments (PI, site, institution, MSA, local vendors, etc.) for assigned projects.
  • Track and oversee contract status, including the dispatch and return of contracts.
  • Negotiate financial and legal conditions and escalate issues as applicable.
  • Act as a single point of contact for local Legal and ERC for patient reimbursement topics.
Requirements:
  • Bachelor's degree required.
  • 2+ years of experience working in clinical trial contracts.
About IQVIA:

IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to improve patient outcomes and population health worldwide.



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