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The Clinical Research Coordinator II’s primary responsibilities are to screen, enroll and follow study subjects ensuring protocol and regulatory compliance and close monitoring while subjects are on study. Due to enhanced experience the CRC II will assume a greater study workload, overall study responsibility, and stronger Sponsor and CRO interaction, while conveying a positive image of Meridien Research to community, sponsors, CROs and study participants and family members. We have positions available in; Decatur-GA, Lakeland-FL, Jacksonville-FL, Deland-FL, and Maitland-FL. PRN and full-time opportunities available.  Essential Functions & Responsibilities: Review and assess protocol (including amendments) for clarity, logistical feasibility,