Clinical Research Coordinator/RN

The US Oncology Network•Denver, CO

5d•Onsite

About The Position

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 in Denver. 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 cliché 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. 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.

Requirements

Associate's degree in a clinical or scientific related discipline required, Bachelor's degree preferred.
Minimum five years of experience in a clinical or scientific related discipline required, preferably in oncology.
SoCRA or ACRP certification preferred.
Graduate from an accredited program for nursing education (BSN preferred).
Minimum seven years of nursing experience, preferably in oncology.
Experience in clinical research preferred.
Current licensure as a registered nurse in state of practice.
Current BLCS or ACLS certification required.
OCN, SoCRA or ACRP certification preferred.
Ability to read, analyze, and interpret technical procedures such as protocols, informed consent documents, and regulatory documents.
Ability to work independently, organize, prioritize, and follow through with results
Ability to solve practical problems and implement solutions
Strong ability multi-task
Must have excellent communication skills
Excellent time management skills
Must have a strong interpersonal skills to be able to interact with multiple people on many different levels
Must have a high level of attention to detail
Must be able to work in a fast paced environment
Attention to details and accuracy
Knowledge of medical terminology, nursing assessment, anatomy and physiology, clinical medical, diagnostic tests, radiology, pathology, pharmacology, hematology, oncology, clinical trials and GCP concepts
Experience with computer data entry and database management
All qualified candidates are required to pass a background check and non-federal drug test (which excludes marijuana) post offer of employment and prior to hire.

Nice To Haves

Bachelor's degree preferred.
SoCRA or ACRP certification preferred.
BSN preferred.
Experience in clinical research preferred.
OCN, SoCRA or ACRP certification preferred.

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 OSHA and the CDC. Maintains strict patient confidentiality according to HIPAA regulations and applicable law.

Benefits

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
employee paid critical illness and accident insurance