Clinical Research Associate

4 days ago


Copenhagen, Copenhagen, Denmark IQVIA Argentina Full time
Job Description

This role involves working as a Single Point of Contact (SPOC) for investigative sites, coordinating with Site Activation Managers (SAMs), Project Management teams, and other departments to ensure compliance with standard operating procedures (SOPs), Work Instructions (WIs), and quality deliverables. The incumbent will perform start-up and site activation activities according to applicable regulations, SOPs, and work instructions.

Key Responsibilities
  • Ensure adherence to regulatory requirements, SOPs, and WIs
  • Perform quality control of documents provided by sites
  • Prepare site regulatory documents, reviewing for completeness and accuracy
  • Distribute completed documents to sites and internal project team members
Qualifications

Candidates must have at least 1 year of clinical research experience.



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