Manager of Clinical Research Operations

Responsibilities

• Oversee and manage daily activities of clinical research nurses, medical assistants, laboratory technicians, and pharmacy staff
• Manage patient enrollment processes, including recruitment, screening, and on-study treatment according to protocol requirements
• Ensure clinical trial activities are completed with accuracy and adherence to Standard Operating Procedures (SOPs)
• Problem-solve daily clinical situations and collaborate with Study Operations to resolve queries, SAEs, and deviations
• Track performance metrics and report monthly findings to leadership
• Lead the hiring, onboarding, and training of the clinical research team
• Manage performance and professional development through quarterly and annual reviews
• Identify opportunities for process improvement and monitor quality outcomes

Requirements

• Associate Degree required (Bachelor Degree preferred)
• Registered Nurse (RN) License to practice in the state of Florida
• At least one year of management experience
• Proficiency in oncology research and clinical operations
• Knowledge of Good Clinical Practices (GCP) and research regulatory guidelines
• Proficiency with Microsoft 365 (Word, Excel, PowerPoint)
• Strong interpersonal, communication, and organizational skills

Preferred Qualifications

• BLS certification

About the Company

Sarah Cannon Research Institute (SCRI) is one of the world’s leading oncology research organizations conducting community-based clinical trials. As a subsidiary of McKesson, SCRI is a leader in drug development, having contributed to pivotal research that has led to the majority of new cancer therapies approved by the FDA in the past decade. Our mission is to transform care and personalize treatment through clinical excellence and cutting-edge research.