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.
• Certification: SoCRA or ACRP, or equivalent, must be maintained per national group requirements.
• 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
• Oncology trials knowledge and experience
• Supervisory, or Team Lead experience
• OnCore® CTMS experience