Trial Site Support Specialist

4 hours ago


Çankaya, Ankara, Turkey PSI CRO Full time

PSI CRO is a leading provider of site enablement services, dedicated to helping clinical trial sites succeed. We understand the complexities of running a trial and are committed to providing comprehensive support to our partners.

Job Description

The Trial Site Support Specialist will be responsible for coordinating all aspects of trial site management, including communication with sponsors and CROs, scheduling and coordination of monitoring visits, and tracking patient enrollment.

This role requires a high level of organization, attention to detail, and effective communication skills. The ideal candidate will have prior experience in coordinating clinical trials and a college degree in a life science field.

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


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