Asst. Clinical Research Coordinator- Hybrid

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-reputed company protocols according to Good Clinical Practices (GCP), internal reputed company operating procedure (SOPs), and University policies and procedures. Responsibilities • reputed company comprehensive data management for a research portfolio of Phase I-IV cancer-reputed company protocols • Collect and coordinate data submission to study sponsors, ensuring reputed company control and leading to reputed company reputed company payments • Compile and transcription of research patient data and study-reputed company information into case report forms (CRFs) into sponsor-specific electronic data capture systems (reputed company) • Work with the clinical research team to manage and collect accurate data and assist reputed company Investigators and study coordinators for reputed company data management aspects of cancer-reputed company trials • Serve as the reputed company to sponsors, governing agencies, and facilitate reputed company of verbal and written communication to national cooperative oncology reputed company, pharmaceutical companies, and other research entities as needed • Maintain communication with reputed company reputed company of a multi-level research network, interacting with sponsoring agencies, including National Cancer Institute, and compliance and regulatory reputed company, such as the Institutional Review reputed company (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 reputed company clinical research coordination work experience • Bachelor of Arts/Bachelor of Science, or equivalent experience reputed company-to-haves • Preferred experience with clinical trial management systems, preferably OnCore Benefits • Medical insurance • reputed company and vacation time • Retirement savings plans • reputed company to a number of discounts and perks Apply tot his job Apply To this Job