Manager of Research EMR Operations

Overview

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 to advance oncology treatments and improve outcomes for cancer patients across the globe. Our mission is to help people who live with cancer, bring the most innovative medical minds together with passionate caregivers, and transform care through clinical excellence and cutting-edge research.

• Manage the team of EMR Analysts to ensure productivity, quality, and timeline metrics are met.
• Serve as a single point of contact for the amendment intake process; manage and review amendment intake.
• Provide scientific and clinical expert interpretation of clinical trial protocols.
• Collaborate with Scientific Director, Physicians, and Program Managers to validate proper protocol interpretation.
• Prepare for the Sarah Cannon Clinical Operations Protocol Review Committee; evaluate protocols, assess complexity, identify risks.
• Create and update the protocol‑specific Clinical Operations worksheet and schedule of events for each patient visit.
• Convert protocol into a schedule of events and maintain it throughout the study life.
• Review and understand all proposed amendments; adjust schedules accordingly.
• Update the Clinical Trial Management System or EMR system with updated schedules to ensure timely notification.
• Provide initial clinical interpretation to each protocol and guide Clinical Educators for consistent interpretation.
• Escalate relevant information to budgets, finance, or Clinical Operations management as needed.

• Extensive oncology knowledge of major cancer types, disease‑related symptom management, standard treatment options, and treatment‑related side‑effect management.
• Knowledge of federal and state regulations and ICH guidelines for clinical trials involving human subjects.
• Understanding of principles, processes, and ethical considerations in clinical trials involving human subjects.
• General working knowledge of Institutional Review Board guidelines, standards, and operating requirements.
• Experience working in a Clinical Trial Management System.
• Bachelor’s Degree;
  Master’s Degree preferred.
• At least three years of experience in oncology.
• At least three years of experience in clinical operations.
• At least three years of research experience.
• RN or BSN preferred.
• Research Certification (ACRP or CCRP) preferred.
• Oncology Certification (OCN) preferred.

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.