Clinical Research Coordinator I, Department of Neurology

Clinical Research Coordinator IThe Department of Neurology at the University of Arizona College of Medicine in Tucson is seeking to recruit a highly motivated research professional to join our clinical research coordinator team in a busy and actively enrolling clinical trial operation. This is an opportunity for individuals with a strong passion for neurological clinical research and advancing the field of neurology, preferably with a background of neurology/neurological research. This position will allow the individual to grow their clinical research skills and apply the acquired knowledge to further their career. Due to the acuity of some of the clinical trials, working on night shifts and weekends is to be expected in a call system. Visa sponsorship is not available for this position. Outstanding U of A benefits include health, dental, and vision insurance plans; life insurance and disability programs; paid vacation, sick leave, and holidays; UA/ASU/NAU tuition reduction for the employee and qualified family members; state retirement plan; access to UA recreation and cultural activities; and more! The University of Arizona has been recognized for our innovative work-life programs.Duties & Responsibilities: Following detailed instructions by the supervisor, assist with promoting/recruiting research participants for long-term clinical trials. Participate in routine recruitment, screening, and enrollment of study participants who meet research eligibility criteria. Help obtain consent forms for approval by Human Subjects Panel. Maintain and update recruitment and screening materials, compliance forms, and tracking documents. Assist with collecting basic information, such as medical histories and assessments interviews, collect and process specimens, answer general questions, fill out case report forms, and help with telephone and in-person contact. Notifies Principal Investigator and supervisor of subject status. Under the direction of the PI and Senior lab members, assist with new protocol submissions, renewals, and revisions to Institutional Review Board for multiple studies. Aid in the submission of study protocols and amendments, consent forms, and recruiting materials to the Institutional Review Board and department for approval with oversight from supervisor. Provide assistance with collecting data, entering and analyzing data, and compiling reports, adhering to proper research protocols. Prepare basic documentation, reports, graphs, and other materials. Keep appropriate logs, tracks participants, and prepares study materials. Under direction of the PI and Senior lab members, assist with coordinating and carrying out daily operations including ordering/maintaining laboratory supplies/equipment. Attend lab meetings.Knowledge, Skills & Abilities: Ability to manage multiple priorities, maintain accurate and detailed records, and meet deadlines in a fast-paced research environment. Strong written and verbal communication skills and proficiency with computer applications used for research documentation and data entry. Ability to work both independently and with a team, resolving issues with a positive outcome. Ability to maintain data accuracy, uphold research integrity, and perform work in accordance with ethical and compliance standards. Ability to contribute to the development of research programs, policies, and procedures and support continuous improvement.Minimum Qualifications: Bachelor's degree or equivalent advanced learning attained through experience required. 1 year of relevant work experience required.Preferred Qualifications: Previous medical experience – highly preferred. Knowledge about neurological disorders, including movement disorders (e.g., Parkinson's disease), seizure disorders (e.g., epilepsy syndromes), and vascular neurological disorders. Passion for neurological research and development of treatments for neurological disorders. Research database experience/certification REDCap, iMedidata. EMR experience (CERNER). Familiar with UA Research Policies. Industry/Government Sponsor knowledge. Familiar with IRB Process.FLSA - ExemptFull Time/Part Time - Full TimeNumber of Hours Worked per Week - 40Job FTE - 1.0Work Calendar - FiscalJob Category - ResearchBenefits Eligible - Yes - Full BenefitsRate of Pay - $47,356 - $59,195.Compensation Type - salary at 1.0 full-time equivalency (FTE)Grade - 6Career Stream and Level - PC1Job Family - Clinical ResearchJob Function - ResearchType of criminal background check required: Name-based criminal background check (non-security sensitive)Number of Vacancies - 1Contact Information for Candidates - Lane StarrettDocuments Needed to Apply - Resume and Cover LetterSpecial Instructions to Applicant - Application: The online application should be completed in its entirety. Blank or missing information may be considered an incomplete submission. Cover Letter: Should clearly indicate how your skills and professional employment experience meet the Minimum and the Preferred qualifications (if applicable).