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Bogotá, Bogotá D.E., Colombia PSI CRO A tiempo completo

At our global company, we value dedication and hard work. As a Clinical Research Site Coordinator, you will have the opportunity to advance your career in clinical research while making a difference in the lives of others.

Responsibilities

Your key responsibilities will include:

  • Being the main point of contact between site personnel and CRA involved in the project.
  • Serving as the primary sites' contact point for vendors, study supplies, and access management.
  • Ensuring that pre-study testing of local site facilities is completed.
  • Assisting Monitors in completing subject event and site event information in CTMS.
  • Managing the order, receipt, inventory storage, distribution, return/recall and reconciliation of clinical supplies.
  • Ensuring regulatory and ethics committee submissions and notifications.
  • Coordinating preparation for and follow-up on site, TMF and systems' audits and inspections.
  • Managing the TMF on a site and a country level.