Assistant Clinical Research Coordinator🔍School of Medicine, Stanford, California, United StatesNew📁Research📅3 days ago Post Date📅105215 Requisition #The Division of Cardiovascular Medicine, in the Department of Medicine, is a dynamic and innovative center dedicated to excellence in research, medical education, and clinical care. Our division is driven by over 80 faculty, clinician educators and instructors who are the pillar of strength in the Division's ongoing efforts in the prevention and treatment of cardiovascular disease.Under the supervision of the Clinical Research Manager and the Principal Investigator, the incumbent is responsible for coordinating clinical trials in the Interventional Cardiology Department. The incumbent is responsible for the timely and accurate collection and coordination of data submission to study sponsors ensuring quality control and leading to timely milestone payments. This includes responsibility for the compilation and transcription of research patient data and study-related information into case report forms (CRFs) into sponsor specific electronic data capture systems (EDC). S/he will work with the clinical research team to manage and collect accurate data and assist Principal Investigators and study coordinators for all data management aspects of their clinical trials. The incumbent is also responsible for maintaining communication with all elements of a multi-level research network, interacting with sponsoring agencies and compliance and regulatory groups such as the Institutional Review Board (IRB), Food and Drug Administration (FDA), and sponsor monitors. In addition, this individual must accurately maintain clinical trial information in the clinical trial management system (OnCore) and adhere to institutional policies.As an Assistant Clinical Research Coordinator, you'll play a key role in supporting the management and coordination of clinical trials and research studies. Working closely with senior team members, you'll help organize tasks, meet deadlines, and ensure compliance with study protocols and regulations. This position offers hands-on experience in a dynamic research environment where your contributions will directly impact the success of clinical projects.Duties include:
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