Share Email Opening Title Clinical Research Coordinator  About the Organization For more than 30 years, IMA has been returning people to work and productivity. IMA is a national leader with three fully integrated divisions: Government Services; Payer Services; and IMA Clinical Research. Diversity is a core value of IMA. Diversity enriches all of us by enhancing our ability to identify challenges, and to discover, design, and deliver solutions. Our Government Services Division supports local, state, and federal agencies and delivers professional and objective medical and psychological examinations as well as ancillary services. Our Payer Services Division meets the evaluation and screening needs of Carriers, TPAs, Public Entities and Employers and includes behavioral health and physical medicine specialty services, working with a wide range of organizations within the workers' compensation, disability, liability, and auto markets. Our Clinical Research Division performs all types of Phase II-IV clinical trials in multiple therapeutic areas through a flexible nationwide network of site locations and virtual capabilities.   Description The IMA Group is seeking to hire a Clinical Research Coordinator for our Clinical Trials location in Phoenix, AZ. The Clinical Research Coordinator position is responsible for supporting clinical research staff and managing new and ongoing clinical research activities. The position includes assisting clinical investigators and research staff to drive projects forward by interacting closely with external clinical research organizations and sponsors, as well as study participants. The Clinical Research Coordinator will adhere to GCP, ICH, and FDA guidelines in the conduct of all study related activities. Duties and Responsibilities: Provide study coordination for assigned trials as directed by the Clinical Research Manager; including data coordination and quality control of research data. Provide back-up and support for all areas of clinical research. Complete regulatory paperwork for IRB submissions, annual reviews and study close-out. Ensure that all Serious Adverse Events (SAEs) are reported in a timely fashion to IRB and sponsor. Create and update Regulatory Binder for each assigned study. Assist with monitoring visits. Interact/liaise with study sponsors and investigators in role of study representative. Conduct eligibility screening interviews over the phone and/or in person. Schedule study patient appointments and make reminder calls to patients; send reminder letters and emails as appropriate. Conduct study patient visits per protocol, including screening and follow-up visits, data collection and entry, specimen collection, and other study activities. Communicate clinical trial status to management and staff through meetings and tracking system; maintain related records. Create and update paper and electronic study patient records. Participate in other recruitment/retention activities as needed, including calling potential participants and occasional outreach. Attend trainings, staff meetings, and in-services as required. Assist lab personnel with specimen processing and shipping as needed. May be asked to attend Investigator Meetings for new trials as assigned. Perform other duties as assigned. Knowledge, Skills and Abilities: Preparation of all study documentation such as protocols, amendments, case report forms, SAE reports and study reports are an integral part of this job. *The above statements are intended to describe the general nature and level of work being performed by people assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities, duties and skills required of personnel so classified.   Location IMA Clinical Research Phoenix   Full-Time/Part-Time Full-Time   EOE Statement We are an equal employment opportunity employer. All qualified applicants will receive consideration for employment without regard to race, creed, color, religion, sex, national origin, disability status, marital or family status, protected veteran status or any other characteristic protected by law.   Benefits Benefits are available including health and prescription, dental insurance, LTD/AD&D/Life Insurance and a discount vision plan. 401K is also offered, as well as PTO (Paid Time Off) and Holiday pay.   This position is currently not accepting applications. 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