Clinical Studies Supervisor

Job Summary

Supervising clinical protocol operations, the full-time Clinical Studies Supervisor will manage and coordinate research activities for Phase 1 clinical trials in a hybrid work environment, ensuring compliance with policies and quality standards while mentoring research staff.

Key responsibilities

• Oversee coordination and facilitation of clinical research activities and patient care protocols
• Supervise and train clinical trials personnel, ensuring adherence to departmental policies and procedures
• Participate in the management of departmental clinical research activities, including performance evaluations and resource utilization

Required qualifications

• Bachelor's degree required; Master's degree preferred
• Six years of experience in research studies or direct patient care, including three years in a supervisory role
• Proficiency in MS Office and strong attention to detail
• Experience in oncology or clinical research preferred
• Successful completion of relevant training programs may substitute for supervisory experience