Oncology Clinical Trials Specialist

JOB SUMMARY:

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.

EDUCATION:
BS required.

EXPERIENCE:

2+ years, professional certification preferred.