Job Title: Clinical Trial SpecialistJob Description
The Clinical Trial Specialist coordinates and supports all aspects of clinical research studies from initiation through activation and ongoing conduct. This role focuses on oncology clinical trials and involves preparing study tools, managing regulatory and sponsor requirements, maintaining accurate research records, and supporting patient screening, enrollment, and follow-up in close collaboration with research nurses, physicians, and other clinical research professionals.
Responsibilities

+ Coordinate the initiation and activation of new clinical trial protocols, ensuring all required approvals are in place before study activation, including Scientific Review Board, Institutional Review Board, Human Research Oversight Committee, data collection plans, and finance/contract approvals.

+ Prepare and organize study tools such as study binders, medication diaries, eligibility checklists, calendars, and flow sheets...