SPVR CLINICAL TRIALS OFFICE Position Available In Hillsborough, Florida
Tallo's Job Summary: Provides basic day-to-day supervision of clinical research staff at H. Lee Moffitt Cancer Center & Research Institute in Tampa, FL. Requires Bachelor's degree in Science or Health care field, SoCRA or ACRP certification, and 4 years of clinical trials experience. Responsible for study start up, trial coordination, quality assurance, and staff management. Full-time position with day shift schedule.
Job Description
SPVR CLINICAL TRIALS OFFICE 3.9 3.9
out of 5 stars 12902 Usf Magnolia Drive, Tampa, FL 33612
Job Summary Position Highlights:
Provides basic day-to-day supervision of the clinical research staff and operations assigned with oversight from responsible CTO manager and in collaboration with faculty and investigators. Works effectively across the organization and externally with sponsor organizations to ensure effective and efficient conduct of clinical research. Supports the recruiting, training, development, and performance management of assigned staff. Operationally focuses on study start up, trial coordination, and quality assurance needs, providing problem-solving and troubleshooting expertise. Will be expected to identify process improvement opportunities, collaborate with their team to develop creative solutions, lead/delegate implementation, and track success through defined metrics.
Responsibilities:
Provide daily supervision of research staff including scheduling to meet program business needs and orientation and training. Supervise the staff responsibilities for the clinical aspects of study start up. Serve as resource to investigators writing investigator-initiated trials. Perform quality assurance procedures to check work of assigned staff for accuracy and completeness. Work with the CTO manager to improve organizational performance through recommending areas or approaches for improvement activities, performing new procedures, collecting data and providing input to department discussions.
Credentials and Qualifications:
Bachelor’s degree. ( Science or Health care related field preferred; Masters preferred ) SoCRA or ACRP (or equivalent) certification. Four (4) years experience in clinical trials (patient facing coordination, data management, regulatory, or other research coordination). Oncology trials knowledge, OnCore CTMS experience preferred. Supervisory, or team lead experience preferred
Location:
H. Lee Moffitt Cancer Center & Research Institute •
Breast Data Mgmt Schedule:
Full Time, Day Shift, Mon – Fri, 8-4:30
