Research EMR Analyst

Sarah Cannon Research Institute

11d

About The Position

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. Our Mission 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. Our Research EMR Analyst interprets clinically the protocol and study documents and transfers this interpretation into the detailed EMR schedule of events and procedures that must be completed with each patient visit. Relocation assistance and visa sponsorship are not available.

Requirements

• Bachelor's Degree required
• RN or BSN (equivalent work experience may be considered in lieu of nursing degree)
• 3+ years' professional work experience in a clinical research setting and/or clinical quality department
• Research work experience should include: Clinical Trial Management System and MS Office Suite
• Knowledge and understanding of the principles, processes, and ethical considerations in clinical trials involving human subjects.
• 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 a general working knowledge of the guidelines, standards, and operating requirements of Institutional Review Boards.

Responsibilities

• Serve as clinical expert in the interpretation of clinical trial protocols and study documents.
• Quality check drug regimens as related to protocols, amendments, and other study documents.
• Work directly with Protocol Educator, Research Coverage Analysts, Scientific Director and/or Physicians, site colleagues, and other supporting teams to validate proper interpretation of the protocol.
• Convert the protocol into a schedule of events of the EMR platform which should be completed with each patient visit during the life of the study.
• Review all proposed amendments and study documents to understand the impact to the clinical trial. And adjust the schedule of events in the EMR to capture any adjustments specified by trial amendments.
• Update CCE and/or Smart Sheets with protocols, amendments, and other study documents.
• Other duties as needed and assigned.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Number of Employees: 501-1,000 employees