Clinical Oncology Research Coordinator

5 days ago


Nashville, Tennessee, United States McKesson Full time
About This Role

We are seeking a highly motivated Clinical Oncology Research Coordinator to join our team at Sarah Cannon Research Institute. As a key member of our research team, you will play a critical role in the coordination and management of clinical trials.

Job Summary

The Clinical Oncology Research Coordinator will be responsible for ensuring protocol compliance, managing study documentation, and coordinating with site staff to ensure timely completion of studies. This is an exciting opportunity to work in a dynamic environment with a passionate team dedicated to advancing cancer care.

Key Responsibilities
  • Ensure adherence to protocol requirements and maintain accurate records
  • Coordinate with site staff to schedule follow-up appointments, scans, and procedures as required by protocol
  • Manage study documentation, including patient files and medication records
  • Communicate effectively with patients, site staff, and sponsors regarding study-related information
  • Participate in regular team meetings to discuss ongoing studies and share best practices
Requirements
  • An Associate Degree; preferably a Bachelor's Degree in a related field
  • RN License and at least one year of oncology experience preferred
  • Knowledge of medical and research terminology, FDA Code of Federal Regulations, and GCP
  • Strong organizational and communication skills, with ability to work independently and as part of a team
What We Offer

Sarah Cannon Research Institute offers a competitive salary range of $63,000 - $83,000 per year, based on experience and qualifications. Our Total Rewards package includes comprehensive benefits, such as medical, dental, and vision insurance, 401(k) matching, and paid time off. We also offer opportunities for professional growth and development, as well as a collaborative and supportive work environment.



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