SPVR CLINICAL TRIALS OFFICE

SPVR CLINICAL TRIALS OFFICE H.

Lee Moffitt Cancer Center - 3.9 Tampa, FL Job Details Full-time 1 day ago Qualifications Clinical supervision Recruitment process management Operations management Faculty collaboration Staff scheduling Research Mid-level Improving operational efficiency Performance management Master's degree Quality assurance Bachelor's degree Data management Team management Staff training Quality improvement Recruiting Healthcare team management Research administration Patient recruitment Oncology 4 years Delegation Staffing management Staff development

Full Job Description 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 •

GI Data Mgmt Schedule:

Full Time, Day Shift, 8:00am-4:30pm