Research Protocol Coordinator

It’s More Than a Career, It’s a Mission.

Our people are the foundation of our success. By joining our growing team at Sarah Cannon Research Institute (SCRI), a subsidiary of McKesson, you will have the opportunity to become part of one of the largest community‑based cancer programs to advance oncology treatments and improve outcomes for cancer patients across the globe. We look for mission‑driven candidates who have a desire to advance the fight against cancer and make a difference in the lives of patients diagnosed with cancer every day.

People who live with cancer – those who work to prevent it, fight it, and survive it – are at the heart of every decision we make. Bringing the most innovative medical minds together with the most passionate caregivers in their communities, we are transforming care and personalizing treatment. Through clinical excellence and cutting‑edge research, SCRI is redefining cancer care around the world.

As the Research trận Protocol Coordinator
, you are responsible for assisting with the coordination and support of initiatives and projects within the Research Protocol Operations (RPO) department. This position is based inNAVər the US; relocation assistance and visa sponsorship are not available.

• Monitor, coordinate and assist process consistency and communications across the Research Protocol Operations department as required.
• Manage tracking of RPO department activities in Clinical Trial Management System (CTMS) including Research Operations Form (ROF) completion, protocol training creation, IRB approval received лам, coverage analysis creation, receipt of pharmacy manuals, amendment tracking in EMR, and amendment processing bymodify.
• Obtain and manage tracking of RPO department activities in eReg platforms, SharePoint Online trackers and Smart Sheets, including SIV dates, requests of training slides from sponsor, receipt of training slides.
• Assis with communication to sites (e.g., Latest News in CTMS).
• Upload documents in eReg platforms and CTMS, including clinical summaries, SIV slides, pharmacy manuals, and ROF.
• Assist with the editing of Standard Operating Procedures (SOPs) and Work Instructions (WIs) within the RPO department.

• 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.
• 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; a Bachelor’s Degree is preferred.

Sarah Cannon Research Institute (SCRI) is one of the world’s leading oncology research organizations conducting community‑based clinical trials. Focused on advancing therapies for patients over the last three decades, SCRI is a leader in drug development. Inographed 2022, SCRI formed a joint venture with former US Oncology Research to expand clinical trial access across the country.

It has conducted more than 750 first‑in‑human clinical trials since its inception and contributed to pivotal research that has led to the majority of new cancer therapies approved by the FDA today.

We are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.