Regulatory Affairs Supervisor, Oncology Trials

Moffitt Cancer Center; Tampa (FL); On-site; USD 85,000 - 110,000; Full time

Job summary

Moffitt Cancer Center in Tampa, FL seeks a Supervisor of Clinical Research Regulatory staff to oversee day-to-day operations, start-up activities, and QA. You will lead recruitment, training, and performance management while identifying process improvements and implementing solutions with measurable results.

The role requires a strong background in clinical research regulatory work, leadership, and proficiency with MS Office; OnCore CTMS experience is highly valued and SoCRA/ACRP certifications

Qualifications

• Bachelor degree plus six years of clinical research regulatory experience.
• High proficiency in Microsoft Excel and Word.
• Demonstrated leadership and team-building abilities.
• OnCore CTMS experience preferred; SoCRA/ACRP certification encouraged.

Responsibilities

• Provide day-to-day supervision of the regulatory staff and operations.
• Support study start-up, trial regulatory, and QA needs.
• Lead recruiting, training, and performance management of staff.
• Identify process improvements and track success with metrics.

Skills

Clinical regulatory exp

Leadership

MS Office

Team building

Education

Bachelor's Degree

Master certification (SoCRA/ACRP)

Tools

OnCore CTMS

Job description

Moffitt Cancer Center in Tampa, FL seeks a Supervisor of Clinical Research Regulatory staff to oversee day-to-day operations, start-up activities, and QA. You will lead recruitment, training, and performance management while identifying process improvements and implementing solutions with measurable results.

The role requires a strong background in clinical research regulatory work, leadership, and proficiency with MS Office; OnCore CTMS experience is highly valued and SoCRA/ACRP certifications