School of Medicine Established in 1930, Duke University School of Medicine is the youngest of the nation's top medical schools. Ranked sixth among medical schools in the nation, the School takes pride in being an inclusive community of outstanding learners, investigators, clinicians, and staff where interdisciplinary collaboration is embraced and great ideas accelerate translation of fundamental scientific discoveries to improve human health locally and around the globe. Composed of more than 2,600 faculty physicians and researchers, nearly 2,000 students, and more than 6,200 staff, the Duke University School of Medicine along with the Duke University School of Nursing, and Duke University Health System comprise Duke Health, a world-class academic medical center. The Health System encompasses Duke University Hospital, Duke Regional Hospital, Duke Raleigh Hospital, Duke Health Integrated Practice, Duke Primary Care, Duke Home Care and Hospice, Duke Health and Wellness, and multiple affiliations. Be You. Participates in or leads day-to-day clinical research data operations conducted by Principal Investigators within the Leukemia Clinical Research Team CRT as part of the Hematologic Malignancies and Cellular Therapies HMCT research groups within Duke Cancer Institute’s DCI Oncology Clinical Research Unit CRU; performs a variety of duties involved in the collection, compilation, documentation, and analysis of clinical research data. May oversee the work of junior staff and train or mentor others in clinical research tasks. Qualifications Required At This Level Education/Training Completion of an Associate’s degree. Experience Work requires a minimum of two years of relevant data experience. A Bachelor’s degree may substitute for two years required experience. Preferences Preferred skills include excellent communication skills, organization, time management, and can easily use computing software and web-based applications e.g., Microsoft Office products and internet browsers. In-dept knowledge and expertise in Phase 1/2 clinical trials eCRF platforms iMedidata Rave, Informs, Zelta, etc; to include Central Imaging platforms Clario, Judi/AG Mednet, Calyx Ambra, etc. Experience with overseeing data management for large oncology portfolio with multiple industry sponsors that utilize a variety of data capture systems. Ability to interpret, evaluate, and explain common procedures/processes as they relate to Hematologic Malignancies, Cellular Therapy, ABMT clinical research trials. Ability to understand, devise, and revise methods needed to assist with overall research support. Bachelor's Degree is strongly preferred. Be Bold. Operations, Study and Site Management – 30% Effort Recognizes when typical agreements MTAs, CDAs, DUAs, DTAs, etc. are necessary and alerts appropriate parties. Knowledgeable in regulatory and institutional policies and processes; applies appropriately in study documentation, protocol submissions, and SOPs. May train
