Oncology Clinical Research Nurse Coordinator

US Oncology Network-wide Career Opportunities; Pueblo (CO); On-site; USD 60,000 - 95,000; Full time

Benefits offered by this job

Health, dental, and vision plans

Wellness program

401(k) retirement plan

Tuition reimbursement

Job summary

Rocky Mountain Cancer Centers in Pueblo, CO seeks an experienced Clinical Research Coordinator/RN to oversee patient screening, enrollment on protocols, and data collection in a dynamic oncology research environment.

Responsibilities include regulatory document maintenance, staff education, and collaboration with physicians on protocol requirements; nursing or CRC background preferred with relevant certifications.

Qualifications

• Minimum five years of experience in a clinical or scientific related discipline, preferably oncology.
• SoCRA or ACRP certification preferred.
• Graduate from accredited nursing program; BSN preferred; seven years nursing experience with oncology preferred.
• Current licensure as a registered nurse in state of practice; BLCS/ACLS as required.

Responsibilities

• Screen potential patients for protocol eligibility and enroll on protocol.
• Coordinate patient care in compliance with protocol requirements; manage investigational drug accountability.
• Data collection, documentation, entry, and reporting; schedule monitoring and auditing.
• Maintain regulatory documents per USOR SOP and applicable regulations.
• Educate clinic staff on clinical research and participate in required training.
• Collaborate with Research Site Leader in study selection and coordinate with sponsors.

Skills

Oncology experience

Clinical research coordination

Regulatory knowledge

Communication skills

Education

Associate's degree in clinical or scientific field

BSN preferred

RN license in state of practice

OCN/SoCRA/ACRP certification preferred

Tools

Computer data entry

Database management

Job description

Rocky Mountain Cancer Centers in Pueblo, CO seeks an experienced Clinical Research Coordinator/RN to oversee patient screening, enrollment on protocols, and data collection in a dynamic oncology research environment.

Responsibilities include regulatory document maintenance, staff education, and collaboration with physicians on protocol requirements; nursing or CRC background preferred with relevant certifications.