Oncology Clinical Trials Specialist

University of Vermont Health Network • Burlington, VT

3d • $53,622 - $84,594 • Onsite

About The Position

The Oncology Clinical Trials Specialist is responsible for managing the study startup timeline and operations requirements for cancer clinical trials in conjunction with the clinical trials office regulatory, clinical, and finance teams and in alignment with department strategic initiatives. Interprets complex research protocols and identifies implicit and explicit items needed for trial activation. Navigates protocols through a complex activation system. Works closely with Regulatory Affairs Supervisor, Clinical Research Supervisor, Regulatory Specialist, and disease teams to support a comprehensive study startup process, goals, and deadlines. Works proactively with various internal and external entities, clinic partners, departments, faculty members, and research collaborators to ensure protocol requirements can be met upon study activation.

Requirements

• BS required.
• 2+ years of experience.

Nice To Haves

• Professional certification preferred.

Responsibilities

• Managing the study startup timeline and operations requirements for cancer clinical trials in conjunction with the clinical trials office regulatory, clinical, and finance teams and in alignment with department strategic initiatives.
• Interpreting complex research protocols and identifying implicit and explicit items needed for trial activation.
• Navigating protocols through a complex activation system.
• Working closely with Regulatory Affairs Supervisor, Clinical Research Supervisor, Regulatory Specialist, and disease teams to support a comprehensive study startup process, goals, and deadlines.
• Working proactively with various internal and external entities, clinic partners, departments, faculty members, and research collaborators to ensure protocol requirements can be met upon study activation.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level