Overview

　　Rocky Mountain Cancer Centers, Colorado's largest and most comprehensiveprovider of cancer care has an exciting opportunity for an experiencedClinical Research Coordinator at our Skyridge location.

　　We realize that it sounds cliche but it is true - taking care of cancerpatients is a calling. It's much more than a job. Each of us has a uniquestory that brought us to Rocky Mountain Cancer Centers (RMCC), but thosestories 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 thephone finding an appointment that fits into a patient's schedule, we aredeeply 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.Hourly range for CRC I Applicants: $25.00-$29.00 Salary Range for CRCII and Sr Applicants: $60,000-$75,000 for non-nurses and$80,000-$95,000 for nuPay is based on several factors including but not limited to education, workexperience, certification, etc.A wide salary range is posted for this position and any job offer is basedupon a salary analysis to comply with the Colorado Equal Pay for Equal WorkAct. The salary analysis considers relevant experience, education, andcertifications as compared to others doing substantially similar work. Whileall 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 onthe salary analysis.As of the date of this posting, in addition to your salary, RMCC offersthe following benefits for this position, subject to eligibilityrequirements: Health, dental, and vision plans; wellness program;health savings account; flexible spending accounts; potential for researchbonus depending on financials of department after one year of employment;401(k) retirement plan; life insurance, short-term disabilityinsurance; long-term disability insurance, Employee Assistance Program;PTO, holiday pay, tuition reimbursement, and employee paid criticalillness andWe will be accepting applications on an ongoing basis for this position. Toapply for this position, start the process by clicking the blue "apply"button.

　　Responsibilities

　　CRC I-Screens potential patients for protocol eligibility. Presents trial conceptsand details to the patients, participates in the informed consent process,and enrolls patients on clinical trials.Assists with patient care in compliance with protocol requirements. Maydisburse investigational drug and maintain investigational drugaccountability. Participates in data collection, entry, and reporting forthe subjects.In collaboration with the physician, reviews patients for changes incondition, adverse events, concomitant medication use, protocolcompliance, response to study drug and thoroughly documents all findings.

　　Participates in required training and education programs as well as monitoringand auditing activities. May work directly with sponsors. May participate inscheduling monitoring and auditing visits, as well as interact with themonitors/auditors while onsite.

　　Assists with collection and maintenance of regulatory documents in accordancewith USOR SOPs and applicable regulations.

　　May assist in the packing and shipping of lab specimens to central vendors.May be required to complete Hazmat and/or IATA training.CRC II-SRScreens potential patients for protocol eligibility. Presents trial conceptsand details to the patients, participates in the informed consent process,and enrolls patients on protocol.Coordinates patient care in compliance with protocol requirements. Maydisburse investigational drug and provide patient teaching regardingadministration. Maintains investigational drug accou tability. -Incollaboration with the physician, reviews patients for changes incondition, adverse events, concomitant medication use, protocolcompliance, 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 auditingactivities.Maintains regulatory documents in accordance with USOR SOP and applicableregulations.Participates in required training and education programs. Responsible foreducation 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 collaborateswith staff in the development of action plans to improve quality.May be responsible for compiling and reporting protocol activity, accrualdata, and research financial information to practice administration andphysicians.May oversee the preparation of orders by physicians to assure that protocolcompliance is maintained. Communicates with physician regarding studyrequirements, need for dose modification, and adverse event reporting.Provides a safe environment for patients, families, and clinical staff atall times through compliance with all federal, state, and professionalregulatory standards as issued through OSHA and the CDC. Maintains strictpatient confidentiality according to HIPAA regulations and applicable law.

　　Qualifications