Clinical Research Coordinator

At American Vision Partners (AVP), we partner with the most respected ophthalmology practices in the country and integrate best-in-class management systems, operational infrastructure, and advanced technology to provide the highest quality patient care possible. Our practices include Barnet Dulaney Perkins Eye Center, Southwestern Eye Center, Retinal Consultants of Arizona, M&M Eye Institute, Abrams Eye Institute, Southwest Eye Institute, Aiello Eye Institute, Moretsky Cassidy Vision Correction, Wellish Vision Institute, West Texas Eye Associates and Vantage Eye Center. We are focused on building the nation’s largest and most comprehensive eye care practices and currently operate more than 100 eye care centers in Arizona, New Mexico, Nevada, California and Texas – including 25 ambulatory surgical centers. At AVP we value teamwork, providing exceptional experiences, continuous improvement, financial strength, and hard work. We are committed to providing best-in-class patient care, pioneering research and technology, and most importantly, rewarding and recognizing our employees! Overview As a Clinical Research Coordinator, you’ll oversee and facilitate the clinical research activities. Responsibilities Coordinates protocol related research procedures, study visits, and follow-up careScreens, recruits, and enrolls patients/research participantsSchedules patient/research participants visits and proceduresIndependently completes the informed consent process of study subjectsEducates research participants and family on protocol, study intervention, study drug/device, etc.Conducts vital signsCollects, processes, and ships laboratory specimensAdministers questionnairesSupports the safety of clinical research procedures, study visits, and follow-up careSubmits documents to regulatory authorities (IRB, FDA, etc.) and/or review/monitoring boardsFacilitates study close out activitiesRetains records and archives documents after conclusion of studyCompletes case report forms and address queriesDevelops and maintains source documentsPerforms additional duties as assigned Qualifications Associates Degree or an allied health professional degree or equivalentAt least 1 year clinical research experience to include consenting patientsBasic understanding of regulatory binders highly preferredAbility to adhere to Good Clinical Practices, FDA, HIPPA, IRB regulation, and principal of research designDetail oriented, reliable and able to multi-task in a fast-paced, high-volume work environmentExcellent verbal and written communication skillsPersonable; empathetic with subject's needs and concernsAbility to maintain confidentiality and professionalismFlexible schedule working Monday-FridayOccasional travel to other RCA location in Metro Valley. Benefits & Perks Your health, happiness and your future matters! At AVP, we offer everything from medical and dental insurance, significant eye care discounts, child care assistance, pet insurance, continuing education funds, 401(k), paid holidays, PTO, Sick Time, opportunity for growth, and much more!