Clinical Study Facilitator

4 hours ago


Çankaya, Ankara, Turkey PSI CRO Full time

We are seeking a highly organized and detail-oriented Clinical Study Facilitator to join our team. In this role, you will be responsible for coordinating all aspects of clinical trial site management, including communication with sponsors and CROs, scheduling and coordination of monitoring visits, and tracking patient enrollment.

Job Requirements

The ideal candidate will have prior experience in coordinating clinical trials, a college degree in a life science field, and excellent communication and problem-solving skills.

We offer a collaborative and dynamic work environment, opportunities for professional growth, and a chance to make a meaningful contribution to the development of new treatments.

Key Responsibilities
  1. Coordinate clinical trial site management
  2. Communicate with sponsors/CROs and trial sites
  3. Schedule and coordinate monitoring visits
  4. Track patient enrollment and support project timelines
  5. Maintain accurate records and data entry into EDC systems
  6. Report and follow up on adverse events and protocol deviations
  7. Handle investigational products and clinical supplies


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