Manages the team responsible for the design, administration, and execution of clinical research trials. Monitors and ensures adherence to established processes and procedures, FDA regulatory requirements, Good Clinical Practice (GCP) research standards, and JCAHO and International Conference on Harmonization (ICH) guidelines. May assist with the development and implementation of clinical processes, procedures, and programs. May require a master's degree. May require ACRP or SOCRA certification. Typically reports to a director. Manages subordinate staff in the day-to-day performance of their jo...View More
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