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Sarah Cannon Research Institute · 1 day ago

Research EMR Analyst

Tennessee, United States

Full-time

Onsite

Mid Level

3+ years exp

Sarah Cannon Research Institute (SCRI) is one of the world’s leading oncology research organizations conducting community-based clinical trials. The Research EMR Analyst interprets clinical trial protocols and study documents, converting them into detailed EMR schedules of events and procedures for patient visits.

Research

No H1B

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

Qualification

Clinical Trial Management SystemOncology knowledgeClinical research experienceMS Office SuiteFederalState regulationsBachelor's DegreeRNBSNSoft skills

Required

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