Clinical Trial Site Coordinator
3 tygodni temu
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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