Senior Regulatory Coordinator (Clinical Research)

Russell Tobin is seeking a Sr. Clinical Research Regulatory Coordinator for a regional health care delivery network. Job Title: Sr. Clinical Research Regulatory Coordinator Location: Newport Beach, CA 92663 (On-Site) Job Type: Direct Hire Est. Start Date: January 6, 2025 Hours: 8:30 am – 5pm Pay Range: $37.38 - $57.46 per hour Job Summary: The Sr. Clinical Research Regulatory Coordinator supports clinical research teams (physicians, nurses, etc.) and with minimal direction and considerable use of independent judgment, facilitates the study start-up approval process and maintaining documentation of regulatory compliance throughout the trial's duration for research studies involving human subjects. The Sr. Regulatory Coordinator ensures all research studies are compliant with regulations and maintains accurate and up-to-date regulatory files. The Sr. Coordinator is the central resource for regulatory staff conducting clinical research. Regarding department supporting: Cancer trials account for approx. 70% of trials. Also support GI, Cardiac, Diabetes and Neurology Essential Duties: Understands current regulatory requirements and ensures a smooth submission process to minimize delays to study initiation. Remains informed of current federal, state, and local regulations regarding clinical research and communicates any changes to study team. Tracks each protocol through the IRB/subcommittee approval process, evaluates for recurrent problems, develops and implements systems to decrease delay in the approval process. Works closely with Investigators and Research Staff on new studies to ensure timely, accurate submissions to the IRB and sponsors. Works with sponsors to ensure all proper regulatory documents are approved and that all documents, access to CRF and databases, monitoring/auditing requirements have been completed prior to the start of a study. Produces and maintains regulatory binders prior to studies starting with all required documents and ensure dedicated electronic study folder is current. Obtains and completes all required documents for new submissions, exemption requests, compassionate uses, amendment applications, continuing review, and closure activities. Completes the External Visitors Checklist to meet badge requirements for access to institution. Reviews informed consents for institutional language and works with legal and sponsors to ensure CTA language is consistent with consent. Works with multiple IRBs and understands submission process and requirements. Provides institutional authorization for new submissions with WIRB. Provides study, enrollment updates, and SAE reports to Clinical Research Oversight Committee. Work with Investigators to renew NCI/CTEP applications. Participates in all investigator meetings, as required. Maintains working knowledge of current protocols and internal SOPs. Assists with the coordination and review of amendments, annual reports, safety reports, and other regulatory submissions required for maintenance of INDs or IDEs. Serves as a team leader within the clinical research regulatory team and trains new regulatory staff, when appropriate. Education: Bachelor’s Degree Experience: 5 yrs minimum of regulatory documentation experience in clinical research required 30-50 clinical trials completed at minimum Experience with opening trials, filing applications and submissions for Phase 1 trials FDA and IRB start up experience. Ability to work in fast paced environments. Experience submitting applications and submissions to IRB (Institution Review Board) Preferred Skills & Experience: Working knowledge of NIH, and OHRP regulatory requirements and ICH GCP guidelines preferred. Apply Today If you are interested in the position, please email your resume to rob.vanrietrusselltobin.com for immediate consideration.