Job Overview
Employment Type
Full-time
Compensation
Type:
Salary
Rate:
Range $80,000.00 - $97,000.00
Work Schedule
Standard Hours
Benefits
Health Insurance
Dental Insurance
Vision Insurance
Wellness Program
Health savings account
flexible spending accounts
401(k) retirement plan
Life insurance
short-term disability insurance
long-term disability insurance
Paid Time Off
Holiday pay
Tuition Reimbursement
critical illness insurance
accident insurance
Employee assistance program
Job Description
Rocky Mountain Cancer Centers (RMCC) stands as Colorado's largest and most comprehensive provider of cancer care, dedicated to offering advanced and compassionate treatment to patients facing cancer. Located in Pueblo, RMCC boasts a team focused on excellence in oncology services, combining cutting-edge research with personalized patient care. This establishment is recognized for its commitment to improving patient outcomes through a supportive and innovative environment, making it a leader in cancer care within the region. RMCC's holistic approach emphasizes not only clinical excellence but also patient-centered service, ensuring every patient feels supported throughout their treatment journey.
The Clinical Research Coordinator/R... Show More
The Clinical Research Coordinator/R... Show More
Job Requirements
- Associate's degree in clinical or scientific related discipline
- minimum five years experience in clinical or scientific related field, preferably oncology
- or graduate from accredited nursing education program
- minimum three years nursing experience, preferably in oncology
- current licensure as registered nurse in state of practice
- current BLS or ACLS certification
- ability to work independently
- excellent organizational and communication skills
- ability to maintain patient confidentiality per HIPAA
- ability to comply with federal and state regulatory standards
- ability to pass background check and non-federal drug test
- proof of influenza vaccination upon employment
Job Qualifications
- Associate's degree in a clinical or scientific related discipline required
- Bachelor's degree preferred
- minimum five years experience in clinical or scientific related discipline, preferably oncology
- SoCRA or ACRP certification preferred
- or graduate from accredited nursing education program, BSN preferred
- minimum three years nursing experience, preferably in oncology
- experience in clinical research preferred
- current licensure as registered nurse in state of practice
- current BLS or ACLS certification required
- OCN, SoCRA, or ACRP certification preferred
- 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
- excellent written and oral communication skills
- excellent organizational skills
- attention to detail and accuracy
- 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
Job Duties
- Screens potential patients for protocol eligibility
- presents trial concepts and details to patients
- participates in the informed consent process
- enrolls patients on protocol
- coordinates patient care in compliance with protocol requirements
- disburses investigational drug and provides patient teaching regarding administration
- maintains investigational drug accountability
- reviews patients for changes in condition, adverse events, concomitant medication use, protocol compliance, and response to study drug
- documents all findings thoroughly
- 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
- educates clinic staff regarding clinical research
- collaborates with Research Site Leader in study selection process
- works directly with non-USOR research bases and/or sponsors
- identifies quality and performance improvement opportunities and collaborates with staff to develop action plans
- compiles and reports protocol activity, accrual data, and research financial information to administration and physicians
- oversees preparation of physician orders to maintain protocol compliance
- communicates with physicians regarding study requirements, dose modifications, and adverse event reporting
- provides a safe environment for patients, families, and clinical staff through compliance with federal, state, and professional regulatory standards
- maintains strict patient confidentiality according to HIPAA regulations and applicable law
Job Qualifications
Experience
Expert Level (7+ years)
Job Location
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