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Clinical Research Coordinator​/RN

Job in Lone Tree, Douglas County, Colorado, 80124, USA
Listing for: US Oncology Network-wide Career Opportunities
Full Time position
Listed on 2026-01-01
Job specializations:
  • Nursing
    RN Nurse, Oncology Nurse
Salary/Wage Range or Industry Benchmark: 80000 - 97000 USD Yearly USD 80000.00 97000.00 YEAR
Job Description & How to Apply Below

Overview

Rocky Mountain Cancer Centers, Colorado's largest and most comprehensive provider of cancer care has an exciting opportunity for an experienced Clinical Research Coordinator/RN at our Skyridge location in Lone Tree.

Bring your established Oncology and or Research experience and join a team dedicated to providing an excellent experience to patients.

We realize that it sounds cliche but it is true - taking care of cancer patients is a calling. It's much more than a job. Each of us has a unique story that brought us to Rocky Mountain Cancer Centers (RMCC), but those stories usually share common themes of care, compassion, and commitment.

No matter the role each RMCC team member serves in, the goal is the same: to provide the best care possible for each and every one of our patients. Whether we are a nurse holding our patient's hand, or a scheduler on the phone finding an appointment that fits into a patient's schedule, we are deeply connected to our patients and do what we can to help.

If this sounds like you, we'd love to have you join our team.

Salary Range: $60,000-$75,000 for non-nurses and $80,000-$97,000 for nurses

Pay is based on several factors including but not limited to education, work experience, certification, etc. As of the date of this posting, in addition to your salary, RMCC offers the following benefits for this position, subject to eligibility requirements:
Health, dental, and vision plans; wellness program; health savings account; flexible spending accounts; potential for research bonus depending on financials of department after one year of employment; 401(k) retirement plan; life insurance, short-term disability insurance; long-term disability insurance, Employee Assistance Program; PTO, holiday pay, tuition reimbursement, and employee paid critical illness and accident insurance.

A wide salary range is posted for this position and any job offer is based upon a salary analysis to comply with the Colorado Equal Pay for Equal Work Act. The salary analysis considers relevant experience, education, and certifications as compared to others doing substantially similar work. While all offers are compliant with the Colorado Equal Pay for Equal Work Act, there is no guarantee an offer will be at the top of the posted range based on the salary analysis.

Responsibilities
  • Screens potential patients for protocol eligibility. Presents trial concepts and details to the patients, participates in the informed consent process, and enrolls patients on protocol.
  • Coordinates patient care in compliance with protocol requirements. May disburse investigational drug and provide patient teaching regarding administration. Maintains investigational drug accountability. In collaboration with the physician, reviews patients for changes in condition, adverse events, concomitant medication use, protocol compliance, response to study drug and thoroughly documents all findings.
  • Responsible for accurate and timely data collection, documentation, entry, and reporting. Schedules and participates in monitoring and auditing activities.
  • Maintains regulatory documents in accordance with USOR SOP and applicable regulations.
  • Participates in required training and education programs. Responsible for education of clinic staff regarding clinical research.
  • May collaborate with Research Site Leader in the study selection process.
  • Additional responsibilities may include working directly with other (non-USOR) research bases and/or sponsors.
  • Identify quality and performance improvement opportunities and collaborates with staff in the development of action plans to improve quality.
  • May be responsible for compiling and reporting protocol activity, accrual data, and research financial information to practice administration and physicians.
  • May oversee the preparation of orders by physicians to assure that protocol compliance is maintained. Communicates with physician regarding study requirements, need for dose modification, and adverse event reporting.
  • Provides a safe environment for patients, families, and clinical staff at all times through compliance with all federal, state, and professional regulatory standards as issued through…
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