SPVR REGULATORY AFFAIRS CTO

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

Working at Moffitt is both a career and a mission: to contribute to the prevention and cure of cancer. As the only National Cancer Institute-designated Comprehensive Cancer Center based in Florida, Moffitt employs some of the best and brightest minds from around the world. Join a dedicated team of nearly 11,000 who are shaping the future we envision. Moffitt has been recognized as a Best and Brightest Company to Work For in the Nation and is continually named one of the Tampa Bay Times’ Top Workplaces.

Summary Job Summary: With oversight from the responsible CTO Manager, and in collaboration with the faculty and investigators, the Supervisor provides basic day-to-day supervision of the clinical research regulatory staff and operations for the research programs assigned with the goal to support program regulatory needs. The Supervisor supports the recruiting, training, development, and performance management of assigned staff. Operationally, the Supervisor focuses on the day to day study start up, trial regulatory, and quality assurance needs, providing problem solving and troubleshooting expertise. The Supervisor 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.

Requirements:

• Bachelors Degree Six (6) years previous clinical research regulatory experience High level competency in Microsoft Office Suite - Excel and Word required Demonstrated leadership and team building skills.
• Demonstrated diplomacy, tact, and professional demeanor.
• Strong collaborative, prioritization and organizational skills.
• Preferred: Masters Degree Certification: SoCRA or ACRP, or equivalent, must be maintained per national group requirements.
• Oncology trials knowledge and experience.
• Supervisory, or Team Lead experience.
• OnCore® CTMS experience.

Salary Range Salary ranges posted for this position represent the expected base pay range for the role. Actual compensation may vary based on location and a variety of job-related factors, including experience, skills, education, and internal equity among Team Members in similar positions. We are committed to maintaining fair and equitable pay practices and regularly review compensation to ensure alignment across our workforce.

Equal Employment Opportunity

Moffitt Cancer Center is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, or protected veteran or disabled status. We seek candidates whose skills, and personal and professional experience, have prepared them to contribute to our commitment to diversity and excellence.

Reasonable Accommodation

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