Sarah Cannon Research Institute
Research Protocol Coordinator
Sarah Cannon Research Institute, Nashville, Tennessee, United States
Mission Statement
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 be part of one of the largest community‑based cancer programs that advance oncology treatments and improve outcomes for cancer patients worldwide.
About the Role As the Research 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 in the US; relocation assistance and visa sponsorship are not available.
Responsibilities
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) to include Research Operations Form (ROF) completion, protocol training creation, IRB approval received, coverage analysis creation, receipt of pharmacy manuals, amendment tracking in EMR, and amendment processing by the education team.
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.
Assist with communication to sites (e.g., Latest News in CTMS).
Upload documents in eReg platforms and CTMS to include clinical summaries, SIV slides, pharmacy manuals, ROF.
Assist with the editing of Standard Operating Procedures (SOPs) and/or Work Instructions (WIs) within the RPO department.
Qualifications
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.
Company Overview 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. In 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. SCRI’s research network brings together more than 1,300 physicians who are actively enrolling patients into clinical trials at more than 250 locations in 24 states across the U.S.
Benefits We care about the well‑being of the patients and communities we serve, and that starts with caring for our people. We offer a Total Rewards package that includes comprehensive benefits to support physical, mental, and financial well‑being. As part of Total Rewards, we offer a competitive compensation package determined by performance, experience, skills, equity, regular job market evaluations, and geographical markets. In addition to base pay, other compensation, such as an annual bonus or long‑term incentive opportunities, may be offered.
Equal Opportunity Employer 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.
#J-18808-Ljbffr
About the Role As the Research 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 in the US; relocation assistance and visa sponsorship are not available.
Responsibilities
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) to include Research Operations Form (ROF) completion, protocol training creation, IRB approval received, coverage analysis creation, receipt of pharmacy manuals, amendment tracking in EMR, and amendment processing by the education team.
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.
Assist with communication to sites (e.g., Latest News in CTMS).
Upload documents in eReg platforms and CTMS to include clinical summaries, SIV slides, pharmacy manuals, ROF.
Assist with the editing of Standard Operating Procedures (SOPs) and/or Work Instructions (WIs) within the RPO department.
Qualifications
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.
Company Overview 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. In 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. SCRI’s research network brings together more than 1,300 physicians who are actively enrolling patients into clinical trials at more than 250 locations in 24 states across the U.S.
Benefits We care about the well‑being of the patients and communities we serve, and that starts with caring for our people. We offer a Total Rewards package that includes comprehensive benefits to support physical, mental, and financial well‑being. As part of Total Rewards, we offer a competitive compensation package determined by performance, experience, skills, equity, regular job market evaluations, and geographical markets. In addition to base pay, other compensation, such as an annual bonus or long‑term incentive opportunities, may be offered.
Equal Opportunity Employer 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.
#J-18808-Ljbffr