Regulatory Coordinator (Remote)

Job Detailsnbowman2023-07-28T09:28:31-07:00

Regulatory Coordinator (Remote)

Work Location Los Angeles,CA

Job #8449

Work Hours Monday – Friday, 8:00am – 5:00pm

Employment Type 2 – Staff: Career

Duration Indefinite

Salary Range $24.28-48.04 Hourly

Posted Date August 22, 2023

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You can find the cures you know are out there. At UCLA Health, you make it happen as part of a groundbreaking Research team, working to understand hundreds of medical disorders and improving processes for dozens of procedures across the globe.

JOB DUTIES

JOB QUALIFICATIONS

JOB DUTIES

Description

Engage in research activities at UCLA Main Campus within the regulatory team situated in Westwood, operating under the guidance of Operational Managers, Investigators, the Financial Administrative Office (FAO), Faculty, Medical and Administrative Directors of the Jonsson Comprehensive Cancer Center (JCCC) Clinical Research Unit (CRU). The role involves the meticulous preparation, submission, and upkeep of regulatory applications essential for ongoing research initiatives. This entails collaborating with Sponsor monitors to ensure the timely processing, review, and collection of regulatory documents preserved within the Investigator Site File. Adherence to good clinical practice (GCP), JCCC CRU standard operating policies (SOP), UCLA Institutional Review Board (IRB) standards, and governmental regulations is imperative in all tasks. Task allocation may come from direct supervisors, investigators, or Senior Management, and these assignments could be subject to modification as required. Flexibility in working hours is necessary to meet the deadlines and priorities of studies and CRU responsibilities. Salary range: $24.28 – $48.04

JOB QUALIFICATIONS

Qualifications

Computer skills using PC platform computers with proficiency in Excel and Word to enter data and generate correspondence accurately. Clinical research experience, with in depth knowledge of clinical oncology as it pertains to clinical trials and studies. Demonstrated working knowledge of current medical terminology specific to oncology, to accurately read entries in patient charts and record accurately and timely, information into study records and other appropriate research data forms. Demonstrated knowledge of “good clinical practices” for clinical research as defined by the Code of Federal Regulations (CFR). Demonstrated knowledge of all components of the research process as it pertains to clinical trials and studies, i.e., IRB procedures and processes, data management, , etc. · Demonstrated English writing skills to generate original correspondence, including reports, using correct grammar, syntax and punctuation. · Demonstrated English verbal skills to obtain and convey accurate information, explaining research protocol to patients and other staff.

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