Clinical Research Coordinator

The US Oncology Network•Littleton, CO

7d•Onsite

About The Position

Rocky Mountain Cancer Centers is hiring an experienced Clinical Research Coordinator/RN in Littleton, Colorado. The position coordinates clinical research and patient care in an oncology setting, supporting protocol enrollment, participant safety, study compliance, accurate research documentation, and education of clinic staff. The role may involve investigational drug handling, communication with physicians and research sponsors, and reporting protocol activity and financial information. The work takes place in an oncology/hematology clinic environment, with potential exposure to communicable diseases, toxic substances, ionizing radiation, medical preparations, and other related conditions. The role requires substantial computer-based work, as well as extended periods of standing and walking and occasional lifting or carrying items up to 40 pounds. The position has two qualification pathways: a clinical or scientific discipline pathway and a registered nurse pathway. Compensation is listed as $60,000–$75,000 for non-nurses and $80,000–$97,000 for nurses. Pay is determined based on factors such as education, work experience, and certifications. Candidates must pass a background check and non-federal drug test after an offer and before hire, and must show proof of influenza vaccination upon commencing employment, subject to reasonable accommodations under applicable law.

Requirements

Associate's degree in a clinical or scientific-related discipline, or graduation from an accredited nursing education program.
For the clinical or scientific pathway: at least five years of experience in a clinical or scientific-related discipline; oncology experience preferred.
For the nursing pathway: at least seven years of nursing experience; oncology experience preferred.
For the nursing pathway: current registered nurse licensure in the state of practice.
For the nursing pathway: current BLCS or ACLS certification.
Ability to read, analyze, and interpret technical procedures, including protocols, informed consent documents, and regulatory documents.
Ability to work independently, organize, prioritize, and follow through.
Ability to solve practical problems and implement solutions; strong multitasking ability.
Excellent communication, time management, and interpersonal skills, including the ability to interact with people at multiple levels.
Strong attention to detail and accuracy; ability to work in a fast-paced environment.
Knowledge of medical terminology, nursing assessment, anatomy and physiology, clinical medicine, diagnostic tests, radiology, pathology, pharmacology, hematology, oncology, clinical trials, and GCP concepts.
Experience with computer data entry and database management.
Ability to meet the physical demands of extended standing and walking, occasional lifting and carrying up to 40 pounds, and corrected vision and hearing within the normal range.

Nice To Haves

Bachelor's degree preferred for the clinical or scientific pathway.
SoCRA or ACRP certification preferred for the clinical or scientific pathway.
Clinical research experience preferred for the nursing pathway.
BSN preferred for the nursing pathway.
OCN, SoCRA, or ACRP certification preferred for the nursing pathway.
Oncology experience preferred.

Responsibilities

Screen potential patients for protocol eligibility; present trial concepts and details, participate in informed consent, and enroll patients on protocols.
Coordinate patient care in compliance with protocol requirements; may disburse investigational drugs and teach patients about their administration; maintain investigational drug accountability.
In collaboration with physicians, review changes in patient condition, adverse events, concomitant medication use, protocol compliance, and response to study drug, and document findings thoroughly.
Collect, document, enter, and report research data accurately and on time; schedule and participate in monitoring and auditing activities.
Maintain regulatory documents in accordance with USOR SOPs and applicable regulations.
Participate in required training and education programs and educate clinic staff about clinical research.
May collaborate with the Research Site Leader in selecting studies.
May work directly with other research bases and sponsors outside USOR.
Identify quality and performance improvement opportunities and collaborate with staff on action plans.
May compile and report protocol activity, accrual data, and research financial information to practice administration and physicians.
May oversee physician order preparation to ensure protocol compliance and communicate study requirements, dose-modification needs, and adverse-event reporting to physicians.
Maintain a safe environment for patients, families, and clinical staff by complying with federal, state, professional, OSHA, and CDC standards.
Protect patient confidentiality in accordance with HIPAA and applicable law.

Benefits

Health insurance plans
Dental insurance plans
Vision insurance plans
Wellness program
Health savings account
Flexible spending accounts
Potential research bonus depending on department financials after one year of employment
401(k) retirement plan
Life insurance
Short-term disability insurance
Long-term disability insurance
Employee Assistance Program
Paid time off
Holiday pay
Tuition reimbursement
Employee-paid critical illness insurance
Employee-paid accident insurance