SPVR CLINICAL TRIALS ACTIVATION

Job Summary:

With oversight from the Manager, Clinical Trial Activation, and in collaboration with the faculty and investigators, the Supervisor provides basic day-to-day supervision and oversight of the assigned clinical research operations program staff to ensure implementation of good clinical practices as set forth by Federal regulations. The Supervisor has direct reporting responsibilities and supports the recruiting, training, development, and performance management of staff. Operationally, the Supervisor focuses on the day-to-day conduct of study activation and quality assurance needs, providing problem solving and troubleshooting expertise. The Supervisor may be expected to identify process improvement opportunities, collaborate with the team to develop creative solutions, lead implementation, and track success through defined metrics.
In addition to supervisory responsibilities, the Supervisor, Clinical Trial Activation, will maintain a percent (%) of effort, as determined by the Manager, Clinical Trial Activation, dedicated to Coordinator Study Activation responsibilities.

Minimum Requirements:

Bachelor's Degree Healthcare, life science or relevant degree.

Bachelor's degree with six (6) years of experience in clinical trials (e.g., patient facing coordination, data management, regulatory or other clinical research coordination) inclusive of two (2) years in clinical trial activation.

SOCRA, CCRP or equivalent