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Asst. Clinical Research Coordinator- Hybrid

Remote, USA Full-time Posted 2025-11-24
About the position Under supervision of the Clinical Research Manager, the Assistant Research Data Coordinator (ARDC) supports the clinical research efforts of the CFCCC by providing comprehensive data management for a research portfolio of Phase I-IV cancer-related protocols according to Good Clinical Practices (GCP), internal standard operating procedure (SOPs), and University policies and procedures. Responsibilities • Provide comprehensive data management for a research portfolio of Phase I-IV cancer-related protocols • Collect and coordinate data submission to study sponsors, ensuring quality control and leading to timely milestone payments • Compile and transcription of research patient data and study-related information into case report forms (CRFs) into sponsor-specific electronic data capture systems (EDC) • 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 cancer-related trials • Serve as the liaison to sponsors, governing agencies, and facilitate transmission of verbal and written communication to national cooperative oncology groups, pharmaceutical companies, and other research entities as needed • Maintain communication with all elements of a multi-level research network, interacting with sponsoring agencies, including National Cancer Institute, and compliance and regulatory groups, such as the Institutional Review Board (IRB), Food and Drug Administration (FDA), and sponsor monitors • Accurately maintain clinical trial information in the clinical trial management system (OnCore) and adhere to institutional policies and external Cancer Center Support Grant guidelines for reporting to the National Cancer Institute (NCI) Requirements • 1-3 years of related clinical research coordination work experience • Bachelor of Arts/Bachelor of Science, or equivalent experience Nice-to-haves • Preferred experience with clinical trial management systems, preferably OnCore Benefits • Medical insurance • Sick and vacation time • Retirement savings plans • Access to a number of discounts and perks Apply tot his job Apply To this Job

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