CTO Phase I Trials Supervisor - Operations & Quality Lead

Moffitt Cancer Center; Tampa (FL); On-site; USD 65,000 - 90,000; Full time

Job summary

Moffitt Cancer Center in Tampa, FL is seeking a CTO Supervisor to oversee clinical research operations, study start-up, trial coordination, and data quality assurance across the protocol life cycle.

You will supervise staff, collaborate with investigators and sponsor organizations, and drive process improvements with defined metrics. A Bachelor's degree, SoCRA/ACRP, and 4 years in trials are required; oncology trials and OnCore CTMS experience preferred.

Qualifications

• Bachelor's degree (Science or Health care related field preferred)
• SoCRA or ACRP certification (or equivalent)
• 4 years experience in clinical trials (patient facing coordination, data management, regulatory, or other research coordination)
• Oncore CTMS experience preferred
• Supervisory or team lead experience preferred

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

Skills

Supervision

Clinical trials coordination

Quality assurance

Data management

SOP development

Education

Bachelor's degree

Tools

OnCore CTMS

Job description

Moffitt Cancer Center in Tampa, FL is seeking a CTO Supervisor to oversee clinical research operations, study start-up, trial coordination, and data quality assurance across the protocol life cycle.

You will supervise staff, collaborate with investigators and sponsor organizations, and drive process improvements with defined metrics. A Bachelor's degree, SoCRA/ACRP, and 4 years in trials are required; oncology trials and OnCore CTMS experience preferred.