Clinical Research Coordinator II, Department of Neurology (Full Time)

This Clinical Research Coordinator II, Department of Neurology (Full Time) position is with University of Arizona in Tucson, AZ. Work with PIs, under moderate guidance, in coordinating activities related to recruitment for clinical trials including recruitment of study participants, conduct interviews, and evaluate potential participants; obtain informed consent, and collect and maintain subject data; perform research subjects’ assessment and Neurologic Rating Scales (NIHSS, mRS, MDS-UPDRS, UDysRS, MoCA, C-SSRS, etc). Provide input into the design, development, execution and initial interpretation of clinical trial protocols, treatment plans, compliance forms, and tracking documents. Conduct research work and perform professional literature reviews to assist the Principal Investigator in designing appropriate research methodologies, techniques, and procedures. Serve as a patient resource for concerns and information. Prepare, coordinate and/or maintain regulatory documentation including IRB submission and approval of new or revised protocols, safety reports and progress reports. Collect and submit the required documentation to the Institutional Review Board, the University, and corporate or government sponsors. Enter and manage study data in compliance with GCP standards Participate in data management design and maintenance. Develop administrative and financial recommendations for department management and PIs for research portfolio review. Oversee quarterly review of all Principal Investigator accounts, performing a strategic analysis of PI research portfolios. Collaborate with the Principal Investigator in the preparation of Human Subjects documentation for NIH and other federally funded grant applications. Create and prepare education materials and training to patients, family members, and clinical staff to assure patient safety and adherence to protocols. Administer and assist in the proper collection, processing, storage, and transport of biological specimens and ensure their handling. Order and maintain supplies required for study kits, track spending in this area, and make day-to-day decisions in support of the study. May mentor and train new staff in preparation and conduct of clinical trials. Knowledge, Skills, and Abilities: Knowledge of the principles, practices, and techniques of research clinical skills. Motivated to provide high quality, compliant research. Skill in maintaining detailed records. Desire to build new program and develop new policies. Ability to work both independently and with a team, resolving issues with a positive outcome. High level of integrity, ethics and professionalism. Strong communication and computer skills. Strong organization skills and significant attention to detail for data entry.