Oncology Clinical Trials Research Nurse

MCKESSON Careers; Denver (CO); On-site; USD 83,000 - 100,000; Full time

Job summary

Sarah Cannon Research Institute (SCRI), a McKesson subsidiary, seeks a qualified Research Nurse to screen, enroll, and monitor study participants across cancer trials, ensuring protocol adherence and data integrity.

You will collect data, manage informed consent, and ensure HIPAA compliance while coordinating visits and procedures across trials. RN license and oncology exposure are preferred; ACRP/CCRP certification is a plus.

Qualifications

• Associate degree; bachelor’s preferred.
• RN license required or active.
• Knowledge of FDA CFR and GCP.
• Knowledge of clinical research processes.
• Oncology knowledge or transplant preferred.
• ACRP/CCRP certification preferred.

Responsibilities

• Screen, enroll and follow study subjects per protocol.
• Ensure protocol compliance and adverse event monitoring.
• Complete data collection and source documentation.
• Accurately document informed consent and HIPAA compliance.
• Compute and document required measurements (BSA, CrCl, etc.).
• Coordinate visits, scans and procedures per protocol requirements.

Skills

Medical and research terminology

Regulatory knowledge (FDA CFR & GCP)

Clinical data collection & documen­tat

Oncology knowledge

Clinical research processes

Education

Associate Degree; Bachelor's preferred

RN License

ACRP/CCRP Certification preferred

Job description

Sarah Cannon Research Institute (SCRI), a McKesson subsidiary, seeks a qualified Research Nurse to screen, enroll, and monitor study participants across cancer trials, ensuring protocol adherence and data integrity.

You will collect data, manage informed consent, and ensure HIPAA compliance while coordinating visits and procedures across trials. RN license and oncology exposure are preferred; ACRP/CCRP certification is a plus.