Clinical Trial Site Coordinator

3 tygodni temu


Warszawa, Mazovia, Polska PSI Pełny etat

Job Description

Contribute to the success of our clinical trials

As a Site Coordinator with PSI, you will play a crucial role in managing clinical trials from initiation to completion. Your primary responsibilities will include:

  • Acting as the main point of contact between the Sponsor or CRO and the medical institution.
  • Building and maintaining strong relationships with medical staff and Sponsor or CRO representatives.
  • Coordinating the evaluation of proposed studies and ensuring timely responses to feasibility questions.
  • Facilitating the scheduling, preparation, and conduct of monitoring visits.
  • Participating in monitoring visits and ensuring compliance with study requirements.
  • Tracking enrollment and supporting the medical site team to meet enrollment targets.
  • Maintaining study-specific and general tracking documents.
  • Ensuring accurate and timely data entry into EDC systems.
  • Reporting and following up on Adverse Events, Serious Adverse Events, and Protocol Deviations.
  • Supporting the proper handling and accountability of investigational products and clinical supplies.

Requirements

  • University degree in Life Science.
  • Certified GCP training.
  • Full proficiency in Polish and intermediate English language proficiency.
  • Proficiency in MS Office applications.
  • Valid category B driver's license.

About this opportunity

This is a great chance to develop new skillsets and grow with our company.



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