Overview

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

　　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: $25.00-$29.00Pay is based on several factors including but not limited to education, workexperience, certification, etc. As of the date of this posting, inaddition to your salary, RMCC offers the following benefits for thisposition, subject to eligibility requirements: Health, dental, andvision plans; wellness program; health savings account; flexiblespending accounts; potential for research bonus depending on financials ofdepartment after one year of employment; 401(k) retirement plan; lifeinsurance, short-term disability insurance; long-term disabilityinsurance, Employee Assistance Program; PTO, holiday pay, tuitionreimbursement, and employee paid critical illness and accident insurance.We 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

　　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.

　　Qualifications

　　Minimum Qualifications:High School diploma required.Associates degree in a clinical or scientific related discipline required,Bachelor's degree preferred.One year of experience in a clinical or scientific related discipline,preferably in oncology preferred.Business Experience -Experience in Microsoft OfficeExperience working with physicians preferredSpecialized Knowledge/Skills -Must have excellent communication skillsExcellent organizational skillsStrong ability to multi-taskExcellent time management skillsMust have strong interpersonal skills to be able to interact with multiplepeople on many different levelsMust have a high level of attention to detailMust be able to work in a fast-aced environmentMay be responsible for basic clinical assessmentsBusiness Experience -Experience in Microsoft OfficeExperience working with physicians preferredExperience working in clinical research is preferredSpecialized Knowledge/Skills

　　Must have excellent communication skillsExcellent organizational skillsStrong ability to multi-taskExcellent time management skillsMust have strong interpersonal skills to be able to interact with multiplepeople on many different levelsMust have a high level of attention to detailMust be able to work in a fast-paced environmentMay be responsible for basic clinical assessmentsWorking Conditions:Traditional office environmentThe work environment characteristics described here are representative ofthose an employee encounters while performing the essential functions of thisjob. Reasonable accommodations will be offered to enable individuals withdisabilities to perform the essential functions. Exposure to communicablediseases, toxic substances, ionizing radiation, medical preparations andother conditions common to an oncology/hematology clinic environment.Physical Requirements (Lifting, standing, etc.) -Large percent of time performing computer based work is required.