Research EMR Analyst - Remote

Overview

The Research EMR Analyst at Sarah Cannon Research Institute plays a crucial role in directing the clinical interpretation of protocols and ensuring the successful execution of clinical trials aimed at improving cancer treatment outcomes.

In Short

• Direct clinical interpretation of research protocols.
• Create detailed schedules for patient visits.
• Work with Scientific Directors and Physicians for protocol validation.
• Attend protocol review committees to assess trial complexities.
• Update clinical trial management systems with schedule adjustments.
• Provide clinical interpretation and training to staff.
• Ensure compliance with federal and state regulations.
• Report necessary metrics on trial progress.
• Collaborate with budget and finance teams on clinical trials.
• Maintain extensive knowledge of oncology and clinical practices.

Requirements

• Extensive oncology knowledge base.
• At least three years of oncology and research experience.
• Knowledge of clinical trial regulations and ethical considerations.
• Bachelor's Degree required; Master’s preferred.
• RN or BSN preferred.
• Research certification (ACRP or CCRP) preferred.
• Oncology certification (OCN) preferred.

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.
• Inclusive work environment with strong values.
• Equal opportunity employer promoting diversity.