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Clinical Trial Coordinator

1 miesiąc temu


Warszawa, Mazovia, Polska PSI Pełny etat

Job Title: Site Coordinator

Job Summary:

We are seeking a highly organized and detail-oriented Site Coordinator to join our team at PSI. The successful candidate will be responsible for coordinating and managing clinical trials at our medical institution.

Key Responsibilities:

  • Act as the primary point of contact between the Sponsor, CRO, and medical institution.
  • Build and maintain strong relationships with medical staff and Sponsor/CRO representatives.
  • Facilitate the evaluation of proposed studies and ensure timely responses to feasibility questions.
  • Assist in scheduling, preparation, and conduct of monitoring visits.
  • Participate in monitoring visits and ensure accurate data entry into EDC systems.
  • Track enrollment and support the medical site team to meet enrollment targets.
  • Maintain study-specific and general tracking documents.
  • Ensure timely data entry and resolution of data clarification queries.
  • Support the timely reporting and follow-up of Adverse Events, Serious Adverse Events, and Protocol Deviations.
  • Manage Investigator and Site payments.
  • Ensure the medical site team completes necessary training prior to involvement in clinical trials.
  • Ensure ongoing quality in clinical trials by ensuring all study procedures are conducted as per study requirements.
  • Participate in the preparation and audit of the medical institution.

Requirements:

  • University degree in Life Science (pharmacy, nursing, or lab analytics).
  • Certified GCP training.
  • Full proficiency in Polish and intermediate English language proficiency.
  • Proficiency in MS Office applications.
  • Valid category B driver's license.

Additional Information:

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