Research EMR Analyst - Remote

Overview

The Research EMR Analyst at Sarah Cannon Research Institute plays a crucial role in interpreting clinical trial protocols and translating them into detailed EMR schedules for patient visits, contributing to the advancement of oncology treatments.

In Short

• Serve as a clinical expert interpreting clinical trial protocols.
• Quality check drug regimens related to protocols and amendments.
• Collaborate with various teams to validate protocol interpretations.
• Convert protocols into EMR schedules for patient visits.
• Review amendments and adjust schedules accordingly.
• Update necessary documentation in CCE and Smart Sheets.
• Work within a community-based cancer program.
• Engage in clinical excellence and cutting-edge research.
• Support the mission to improve cancer patient outcomes.
• Participate in a diverse and inclusive work environment.

Requirements

• Bachelor's Degree required; RN or BSN preferred.
• 3+ years of experience in clinical research or quality departments.
• Knowledge of Clinical Trial Management Systems and MS Office Suite.
• Extensive oncology knowledge of major cancer types.
• Understanding of federal/state regulations and ICH guidelines.
• General knowledge of Institutional Review Board guidelines.
• Strong communication and collaboration skills.
• Attention to detail and quality assurance capabilities.
• Ability to adapt to changes in protocols and study documents.
• Commitment to the mission of improving cancer care.

Benefits

• Comprehensive benefits package for physical, mental, and financial well-being.
• Competitive compensation package based on performance and experience.
• Opportunities for professional growth and development.
• Supportive work environment focused on employee health and diversity.
• Participation in meaningful work that impacts patient lives.