Clinical Research Data Manager 1

About The Unit: The Section of Hematology/Oncology has a proud and long tradition of excellence in research-based patient care and clinical discovery. Ranked among the finest cancer programs in the country, the Section is comprised of nationally and internationally known faculty with expertise in all major types of malignancies, blood disorders, and experimental therapies. Major emphasis is given to translational research and the investigation of important laboratory observations in the clinic. One of the only institutions to have clinical trials in Phase I, II, and III of drug development, the distinguished faculty have ongoing investigations in each of these phases.

Unit Job Summary: The Clinical Research Data Manager 1 is responsible for meticulous and accurate clinical data management for each clinical trial. This includes: all patient data retrieval in its various forms(in-house/outside - prior histories, hospital floor admissions, ER visits, Clinic exams, MD office records, Scans, Pathology and Cytology, etc.), the preparation and maintenance of clinical research charts for each protocol patient, timely/daily retrieval, identification and entry of clinical research data into computer program databases, spreadsheets, chart flowsheets, and case report forms. Preparation and routine updating of weekly program conference lists, attendance at multidisciplinary conferences and workshops, schedule, prepare and participate in all pharmaceutical site visits, assist Research Nurse(s) and appropriate departmental, and laboratory staff in collection, storage, and shipment of patient specimens, radiology scans, reports, etc.

Unit Education: Associates degree or an equivalent combination of relevant education & experience required. Bachelor's degree preferred.

Unit Experience: A minimum of one year of relevant clinical research experience preferred.

Unit Job Function Competencies: Ability to facilitate query resolution with sponsor/monitors required. Ability to handle competing demands with diplomacy and enthusiasm required. Strong data management skills and attention to detail required. Ability to work collaboratively across study teams required. Knowledge of Microsoft Word, Excel and Adobe Acrobat required. Ability to maintain a high degree of confidentiality with clinical data and client's proprietary data required. Adaptability to changing working situations and work assignments required. Ability to work independently and as part of a team required. Analytical skills required. Ability to abstract subject data from medical record/source documentation and enter into care report forms and/or databases preferred. Knowledge or interest in a scientific field preferred. Knowledge of medical or /clinical trial terminology preferred.