Regulatory Affairs Supervisor — Oncology Trials Leader

SPEROS; Tampa (FL); Hybrid; USD 90,000 - 120,000; Full time

Job summary

Moffitt Cancer Center in Tampa, FL, is seeking a Senior Supervisor to oversee the clinical research regulatory staff and operations across assigned programs. You will support study start-up, regulatory submission, and quality assurance while guiding recruitment, training, and performance development.

The role emphasizes process improvement, problem solving, and metrics tracking, with collaboration across faculty and investigators to meet program regulatory needs and maintain high standards of

Qualifications

• Bachelor's degree and 6 years of clinical research regulatory experience.
• Strong proficiency in Microsoft Office (Excel and Word).
• Demonstrated leadership and team-building skills.
• OnCore CTMS experience.

Responsibilities

• Provide day-to-day supervision of the clinical research regulatory staff and operations.
• Support recruiting, training, development, and performance management of assigned staff.
• Oversee day-to-day study start-up, trial regulatory, and quality assurance needs.
• Identify process improvement opportunities and track success through defined metrics.

Skills

Clinical research regulatory

Leadership

Team management

Diplomacy

Microsoft Excel

Microsoft Word

Education

Bachelor's degree

Master's degree (SoCRA/ACRP preferred)

Tools

OnCore CTMS

Job description

Moffitt Cancer Center in Tampa, FL, is seeking a Senior Supervisor to oversee the clinical research regulatory staff and operations across assigned programs. You will support study start-up, regulatory submission, and quality assurance while guiding recruitment, training, and performance development.

The role emphasizes process improvement, problem solving, and metrics tracking, with collaboration across faculty and investigators to meet program regulatory needs and maintain high standards of