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Clinical Research Coordinator II
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Full-time
- Clinic Research Coordinator II The Clinical Research Coordinator II , will ensure that quality research is conducted at the assigned investigative sites in accordance with the sponsor protocol, FDA Regulations, and ICH/GCP guidelines and to provide the best quality data to the sponsor.
- The CRC I will also ensure study enrollment meets or exceeds Sponsors' expectations.
- Duties & Responsibilities: Completing all the DMCR-required training, including but not limited to ICH-GCP Certification and IATA Certification on a timely basis.
- Sponsor-provided and IRB-approved Protocol Training b.
- Sponsor-specified EDC and/or IVRS and any other relevant Electronic Systems training.
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