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Clinical Trial Manager II serves as the primary point of contact for clinical trials site operations. In this position, you will be responsible for ensuring compliance with CPC SOPs, Good Clinical Practice guidelines, and applicable federal, state, and local regulations. You will also oversee site management, including the review of monitoring visit reports, site-specific Informed Consent Forms, and the maintenance of required records for monitoring activities. This role requires excellent organizational skills and the ability to manage multiple tasks simultaneously.