Aktualne oferty pracy związane z Clinical Trial Coordinator - Warszawa, Mazovia - PSI
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Clinical Trial Coordinator
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Warszawa, Mazovia, Polska PSI Pełny etatJob Title: Clinical Trial CoordinatorJob Summary:We are seeking a highly skilled Clinical Trial Coordinator to join our team at PSI. The successful candidate will be responsible for coordinating clinical trials, ensuring timely and accurate data entry, and maintaining effective communication with sponsors and medical institutions.Key...
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Clinical Trial Coordinator
4 tygodni temu
Warszawa, Mazovia, Polska PSI Pełny etatJob Title: Clinical Trial CoordinatorJob Summary:We are seeking a highly skilled Clinical Trial Coordinator to join our team at PSI. The successful candidate will be responsible for coordinating clinical trials, ensuring compliance with regulatory requirements, and maintaining effective communication with stakeholders.Key Responsibilities:Coordinate clinical...
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Clinical Trial Coordinator
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Clinical Trial Manager
3 tygodni temu
Warszawa, Mazovia, Polska CDS Fortrea Inc. Pełny etatAt CDS Fortrea Inc., we are seeking a skilled Project Manager Study-Start-Up to join our team in Poland. This full-time position is dedicated to a single sponsor and involves managing country deliverables, timelines, and results for assigned protocols.Your Responsibilities: Execute and oversee clinical trial country submissions and approvals for assigned...
Clinical Trial Coordinator
1 miesiąc temu
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.