Job Information
University of Cincinnati Clinical Research Professional, UC Cancer Center, Office Based Coordinator in Cincinnati, Ohio
Clinical Research Professional, UC Cancer Center, Office Based Coordinator Current UC employees must apply internally via SuccessFactors > Founded in 1819, the University of Cincinnati ranks among the nation's best urban public research universities. Home to more than 50,000 students, 11,000 faculty and staff and 340,000 alumni, UC combines a Top 35 public research university with a physical setting The New York Times calls "the most ambitious campus design program in the country." With the launch of Next Lives Here, the Cincinnati Innovation District, a $100 million JobsOhio investment, nine straight years of record enrollment, worldwide leadership in cooperative education, a dynamic academic health center and entry into the Big 12 Conference, UC's momentum has never been stronger. UC's annual budget tops $1.65 billion and its endowment totals $1.8 billion. The University's overall regional economic impact exceeds $10.6 billion, paving the way for the future of Cincinnati. Job Overview As one of the oldest medical schools in the country, the University of Cincinnati College of Medicine (COM) has a reputation for training best-in-class health care professionals and developing cutting-edge procedures and research that improves the health and clinical care of patients. In partnership with the UC Health academic healthcare system and Cincinnati Children's Hospital Medical Center, College of Medicine's faculty are transforming the world of medicine every day. The University of Cincinnati Cancer Program is looking to fill a patient facing position as a Clinical Research Professional. This position will support the University's mission and commitment to excellence in our students, faculty, staff and all our activities. Under general supervision of the Clinical Research Manager, the Clinical Research Professional provides data management support and assistance to the University of Cincinnati Cancer Center Clinical Trials Office. Duties can span a broad range of activities or be primarily focused within one or more areas of the clinical research spectrum. Please note this is a FULL-TIME, ON-SITE position, with incidental work from home opportunities. Essential Functions Complete training and follow established CTO workflows and CTO/UC Health standard operating procedures. Proactively review and locate source documentation for all study procedures, including, but not limited to, lab work, CT scans, MRIs, ECHOs, eye exams, physical exams, oral, IV, or intratumoral drug administrations, pulmonary function tests, cardiac stress tests, biopsies. Accurately enters data from source documentation listed above, outside hospital records, and/or hard-copy research-specific documents, into study specific electronic data capture (EDC) systems for clinical research trials within 5 days of the patient visit EDCs include, but are not limited to, RedCap, Inform, Medidata Rave, Viva Vault, and Trial Master. Proactively seeks to promptly resolve outstanding data queries and any issues relating to missing or incomplete source documentation through collaboration with clinical research coordinators (CRCs). Reviews all data entered EDCs and subject charts to identify and help resolve any general quality issues with CRCs and quality assurance (QA) staff as needed. (i.e., data collected per protocol and meets GCP, ALCOA standards etc...). Conducts study participant follow-up as required per protocol. Communicates and collaborates within assigned research team and with principal investigators in a professional, helpful, and service-oriented manner to effectively accomplish job duties. Acts as the primary point of contact for monitoring visits - ensuring monitors have access to records, facilities, and remaining available for questions for the duration of a visit. Assists the PRMC/DSMB Coordinator or other QA staff with projects