Inaugural Director-Clinical and Data Coordinating Center Below you will find the details for the position including any supplementary documentation and questions you should review before applying for the opening. To apply for the position, please click the Apply for this Job link/button. Recruitment/Posting Title: Inaugural Director-Clinical and Data Coordinating Center Department: Institute for Translational Medicine and Science The successful candidate will be a national and international leader to develop, direct, coordinate and orchestrate a Center devoted to the establishment of Rutgers Health ( RH ) as a leader in performance and data coordination of multisite clinical trials and observational studies. RH has successfully established national programs in translational research and cancer research with the successful and continued funding of both The New Jersey Alliance for Clinical and Translational Science ( NJ ACTS )—an alliance among Rutgers, Princeton, NJIT and RWJBarnabas Health System, the only CTSA Hub in New Jersey—as well as the Rutgers Cancer Institute (the only NCI designated Comprehensive Cancer Program in New Jersey). These substantial programs provide unprecedented resources for the development of world-class clinical research programs across the state and beyond. The growth of clinical research across Rutgers Health has been meteoric and we are poised to expand our capabilities to include the coordination of national clinical research networks. Rutgers Health is seeking an experienced scientist to lead the Clinical and Data Coordinating Center ( CDCC ). This individual will procure, manage and coordinate NIH-funded and industry-sponsored networks and multicenter trials and cohort studies. Additionally, he/she will leverage current staff and recruit database administrators, data managers, software developers, project managers, clinical monitors, scientists, and research administrators. The Director will be jointly appointed as an Associate or Full Professor in an appropriate department within Rutgers Robert Wood Johnson Medical School and/or School of Public Health and as a senior member of Rutgers Institute for Translational Medicine and Science ( RITMS ). Rank will be commensurate with experience. Applicants must have a M.D., Ph.D. or equivalent degree. The Director will work closely with the RITMS Director to run the CDCC effectively by streamlining operations and budgets and implementing new ideas. The CDCC Director will collaborate with clinician-scientists across Rutgers Health to identify opportunities for sponsored research, and on the submission of applications for their funding. Generous salary and start-up support are available. Resources for the Director of Clinical and Data Coordinating Center: The Clinical and Data Coordinating Center (CDCC) will be established within the Rutgers Institute for Translational Medicine and Science (RITMS). The Director of the CDCC will report to Dr. Reynold Panettieri, Vice Chancellor for Translational Medicine and Science. The CDCC will be provided financial management and administrative support through the RITMS. Expectantly, the CDCC will leverage the current established NJ ACTS Cores concerning Regulatory Affairs and Biostatistics, Epidemiology and Research Design. Additionally, the CDCC Director will have access to the resources and personnel of the Clinical Trials Office, a Chancellor-supported office that coordinates all aspects of clinical research through 5 clinical research units geographically located across NJ, OnCore Enterprise (a Clinical Trials Management System) and Deep6 (a NLP/AI/ML structured and unstructured cohort builder using our Epic EHR). Startup resources will also be provided to recruit a team designed by the Director. Position Status: Full Time Qualifications Minimum Education:

The following information aims to provide potential candidates with a better understanding of the requirements for this role. MD, PhD, or equivalent degree Minimum Qualifications and Experience: Candidates must have substantial experience designing and leading large, extramurally funded, multicenter clinical research network projects, involving clinical trials, cohort studies, and/or registries. They must have experience working in cross-functional study teams, including those functions necessary for successful and innovative data coordinating centers, such as data management systems and operations, reporting for data monitoring committees, clinical research coordination and clinical monitoring, and quality control procedures. Preferred Qualifications: They should have a track record of extramurally funded research in the conduct of clinical trials or cohort studies, and possibly methodologic research into approaches such as adaptive designs, methods for missing data, analytical procedures for causal inference, and statistical monitoring approaches. Additional Qualifications: In addition, successful candidates should have excellent communication skills and administrative acumen, and the ability to work effectively in a clinical and academic environment. Physical Demands and Work Environment: Standing, sitting, walking, talking or hearing. No special vision requirements. Rutgers University: Rutgers, The State University of New Jersey, stands among America’s highest-ranked, most diverse public research universities. The oldest, largest, and top-ranked public university in the New York/New Jersey metropolitan area, its main locations are in three New Jersey cities (New Brunswick, Newark, and Camden). Rutgers University has a prominent academic and clinical health sciences presence that spans across the state, and its footprint is seen around the region. For more information about Rutgers University, please visit: https://www.rutgers.edu/ For more information about Rutgers Health, please visit: https://rutgershealth.org/ All offers of employment are contingent upon successful completion of all pre-employment screenings. It is university policy to provide equal employment opportunity to all its employees and applicants for employment regardless of their race, creed, color, national origin, age, ancestry, nationality, marital or domestic partnership or civil union status, sex, pregnancy, gender identity or expression, disability status, liability for military service, protected veteran status, affectional or sexual orientation, atypical cellular or blood trait, genetic information, or any other category protected by law.

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