Oncology Clinical Research Coordinator: Drive Cancer Trials

McKesson’s Corporate; Nashville (TN); On-site; USD 60,000 - 75,000; Full time

Benefits offered by this job

Total Rewards package

Job summary

Sarah Cannon Research Institute (SCRI) is seeking a Clinical Research Coordinator to manage clinical operations for the facility’s research program, including enrollment, regulatory, quality, and site operations. You will support enrolling patients onto trials through recruitment, screening, enrollment, treatment, and follow-up per protocol.

You will review study designs with physicians, ensure informed consent, and maintain accurate regulatory and data documentation across CRFs or EDC systems,

Qualifications

• Knowledge of medical and research terminology
• Knowledge of FDA Code of Federal Regulations and GCP
• Knowledge of the clinical research processes
• Public presentation skills
• Ability to manage multiple priorities with a diverse team

Responsibilities

• Oversee enrollment, regulatory, quality, and site operations of the research program.
• Support enrolling patients onto clinical trials through recruitment, screening, enrollment, treatment and follow-up.
• Review study design and inclusion/exclusion criteria with physicians and patients.
• Verify informed consent procedures and adherence to protocol requirements.

Skills

Medical terminology

GCP knowledge

Regulatory knowledge

Multitasking

Public presentation

Education

Associate’s Degree

Job description

Sarah Cannon Research Institute (SCRI) is seeking a Clinical Research Coordinator to manage clinical operations for the facility’s research program, including enrollment, regulatory, quality, and site operations. You will support enrolling patients onto trials through recruitment, screening, enrollment, treatment, and follow-up per protocol.

You will review study designs with physicians, ensure informed consent, and maintain accurate regulatory and data documentation across CRFs or EDC systems,