Note: The job is a remote job and is open to candidates in USA. Sarah Cannon Research Institute (SCRI) is a leading oncology research organization focused on advancing therapies for patients. As the Manager of Research EMR Operations, you will manage a team of EMR Analysts to ensure productivity and quality in the clinical interpretation of protocols while developing interdepartmental relationships and overseeing protocol builds.

Responsibilities
• You will manage the team of EMR Analysts to ensure productivity, quality and timeline metrics are met
• You will develop relationships between departments to ensure protocol impacts are communicated out
• You will review protocol builds for accuracy, thoroughness, compliance, and sufficiency
• You will manage the amendment intake process in which the team acts as a single point of contact
• You will serve as scientific and clinical expert in the interpretation of clinical trial protocols
• You will work directly with Scientific Director and/or Physicians and/or Program Managers to validate proper interpretation of the protocol
• You will prepare for the Sarah Cannon Clinical Operations Protocol Review Committee by evaluating and assessing presenting protocols in advance to determine complexity, identify risks associated with a trial and operational and implementation challenges
• You will create and update the protocol specific Clinical Operation worksheet with pertinent study information to use as a study lead tool for Sarah Cannon Clinical Operations and applicable sites
• You will attend the Sarah Cannon Clinical Operations Protocol Review Committee to capture any details presented by the clinical and budget teams
• You will convert the protocol into a schedule of events which should be completed with each patient visit during the life of the study
• You will review all proposed amendments to understand the impact to the clinical trial. Adjust the schedule of events to capture any adjustments specified by trial amendments
• You will update the Clinical Trial Management System or EMR system with the original or updated schedule of events to ensure timely notification to impacted parties
• You will provide initial clinical interpretation for each protocol and guide the Clinical Educators to insure consistent interpretation across the organization
• You will escalate all appropriate information to budgets, finance, or Clinical Operations management as deemed necessary

Skills
• Must have extensive oncology knowledge base of all major cancer types including disease related symptom management, standard treatment options, and treatment-related side effect management
• Must have knowledge of federal and state regulations and ICH guidelines pertaining to the conduct of clinical trials involving human subjects for Investigator and Sponsor requirements
• Must have knowledge and understanding of the principles, processes, and ethical considerations in clinical trials involving human subjects
• Must have a general working knowledge of the guidelines, standards and operating requirements of Institutional Review Boards
• Must have experience working in a Clinical Trial Management System
• You should have a Bachelor's Degree
• At least three years of experience in oncology
• At least three years of experience in clinical operations
• At least three years of research experience
• Master's Degree is preferred
• RN or BSN is preferred
• Research Certification (ACRP or CCRP) preferred
• Oncology Certification (OCN) preferred

Benefits
• Total Rewards package that includes comprehensive benefits to support physical, mental, and financial well-being
• Competitive compensation package
• Annual bonus or long-term incentive opportunities may be offered
• Benefits through our parent company, McKesson

Company Overview
• Sarah Cannon Research Institute is one of the world’s leading oncology research organizations conducting community-based clinical trials. It was founded in 1993, and is headquartered in Nashville, Tennessee, USA, with a workforce of 501-1000 employees. Its website is https://www.scri.com.