Company Highlights:
*Fast growing clinical research site network
*Opportunities for growth and promotion
*Great benefits and culture!
Position: Clinical Research Coordinator III (Full-Time/Non-Exempt)
CRC-III is the most senior clinical research coordinator at our client. They are responsible for the overall management of a high volume of studies including administrative duties and regulatory functions. The CRC III is responsible for clear and direct communication with study sponsor, study monitor, CRO, PI and site manager. Adherence to their SOPs is required. The CRC-III mentors and trains both CRC-I and CRC-II roles and is a resource for high level problem solving and planning of clinical trials. The CRC-III should require minimal direct oversight, fully owning all assigned clinical trials from startup to closeout and meeting enrollment goals. It is the responsibility of the CRC III to represent himself/herself and the site in the most professional, ethical and positive manner.
Reports to: Site Manager
Job Description:
Required Skills/Abilities:
Education and Experience:
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