Clinical Research Coordinator I, Cancer Center

Role of Clinical Research Coordinator: Learn how to apply Good Clinical Practice (GCP)and the Code of Federal Regulations to coordinate the patient care requirements of IRB approved clinical trials protocols. This includes consenting, re-consenting, screening, scheduling appointments and procedures, collecting documentation, and submission of data. Work through protocol eligibility criteria and learn the requirements for registering a patient to a study or clinical trial.Learn to conduct and participate in Site Evaluation Visits (SEV), Site Initiation Visits (SIV), monitoring visits and audits for Investigator Initiated trials (IITs), sponsored studies and cooperative group trials. Participate in trainings, staff meetings and monitoring visits: This includes training from the Clinical Trials Office, University of Arizona, Banner and Sponsors to stay informed of processes and procedures. Willing to be trained in phlebotomy and/or vitals collection through our clinical partner. Perform Data Management tasks: Following ALCOA-C guidelines, all data collected must be attributable, legible, contemporaneous, original and accurate. Coordinators collect, organize and enter data into different data management systems including our local clinical trials management system, the electronic medical record system and specific electronic data capture systems. Gain access to all associated clinical trial data management systems.Collect appropriate signatures to stay in compliance with GCP.Learn to evalute tumor response with Response Evaluation Criteria in Solid Tumors (RECIST) and other evaluation criteria used in Oncology.Learn to follow up on monitoring report action items and queries.Assist in archiving procedures, if necessary. Assist with patient care: Learn to instruct and counsel patients and family members in research procedures. This includes assisting with giving report to pharmacy and infusion nurses for clarification on each specific patients status on each protocol. Learn to read and follow clinical trial protocol calendars and meet all requested time points.Follow protocol compliance by following a patient through all requirements of assigned protocols.Schedule patient visits as needed. Maintain proper communication within the department: Constant communication is required between clinic staff, research RNs, Pharmacokinetic team member, study monitors, and physicians.Patients must be regularly informed of their appointments and research specific requirements (example: additional visits for blood draws and other biological specimen submissions). Learn to work with finance, at UArizona and our Clinical Partner, to appropriately navigate the coverage analysis and charges associated with clinical trials. Other tasks as assigned. Knowledge, Skills & Abilities: Demonstrated strong interpersonal, communication, and problem solving skills.Excellent organizational skills.Attention to detail, including the ability to review information for accuracy, completeness, and consistency.Ability to multitask using time management skills.Ability to navigate electronic databases.