Clinical Research Coordinator

5 hours ago


Fatih, Istanbul, Turkey IQVIA Full time
About the Role

This position plays a critical role in ensuring the successful execution of clinical studies at investigative sites.

Key Responsibilities
  1. Serve as Single Point of Contact (SPOC) for assigned studies, providing timely and accurate support to site staff.
  2. Evaluate and Maintain Compliance with Standard Operation Procedures (SOPs), work instructions (WIs), quality of designated deliverables, and project timelines.
  3. Perform Regulatory Start-up and Maintenance Activities, adhering to applicable regulations, SOPs, and WIs.
  4. Distribute Completed Documents to sites and internal project team members.
  5. Prepare Site Regulatory Documents, reviewing for completeness and accuracy.
  6. Negotiate Site Contracts and Budgets with sites, ensuring agreement on project planning and timelines.
  7. Maintain Internal Systems and Databases, accurately completing and updating project-specific information.
  8. Analyze Site Performance Metrics, providing feedback to management on progress and areas for improvement.
  9. Coordinate Project Planning and Timelines, establishing monitoring measures and contingency plans as needed.
  10. Communicate Progress Updates to team members on completion of regulatory and contractual documents.
  11. Track Document Progress and Approval, ensuring compliance with project timelines.
  12. Collaborate with RSU Leads and Project Teams on initial and ongoing project planning.
  13. Verify Quality Control of documents provided by sites.
  14. Establish Relationships with sponsors and sites, facilitating communication and collaboration.


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