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Sarah Cannon Research Institute · 18 hours ago

Research Protocol Coordinator

Tennessee, United States

Full-time

Onsite

New Grad, Entry Level

Sarah Cannon Research Institute (SCRI) is a leading oncology research organization focused on advancing therapies for cancer patients. The Research Protocol Coordinator is responsible for coordinating and supporting initiatives within the Research Protocol Operations department, ensuring process consistency and communication across the team.

Research

No H1B

Responsibilities

You will monitor, coordinate and assist process consistency and communications across the Research Protocol Operations department as required

You will manage tracking of RPO department activities in Clinical Trial Management System (CTMS) to include Research Operations Form (ROF) complete, protocol training creation, IRB approval received, coverage analysis creation, receipt of pharmacy manuals, amendment tracking in EMR, amendment processing by education team

You will obtain from sponsor & manage tracking of RPO department activities in eReg platforms, SharePoint Online trackers and SmartSheets to include: SIV dates, request of training slides from sponsor, receipt of training slides

You will assist with communication to sites (ex. Latest News in CTMS)

You will upload documents in eReg platforms and CTMS to include clinical summaries, SIV slides, pharmacy manuals, ROF

You will assist with the editing of Standard Operating Procedures (SOPs) and/or Work Instructions (WIs) within RPO department

Qualification

Oncology knowledgeClinical Trial Management SystemFederalState regulationsInstitutional Review BoardsMS OfficeCommunication skillsTeam collaborationAttention to detail

Required

Extensive oncology knowledge base of all major cancer types including disease-related symptom management, standard treatment options, and treatment-related side effect management

Knowledge of federal and state regulations and ICH guidelines pertaining to the conduct of clinical trials involving human subjects for Investigator and Sponsor requirements

Knowledge and understanding of the principles, processes, and ethical considerations in clinical trials involving human subjects

A general working knowledge of the guidelines, standards, and operating requirements of Institutional Review Boards

Experience working in a Clinical Trial Management System and MS Office

An Associate's Degree is required