Job Title

Job Description:Biopharma Informatic is seeking an experienced Clinical Research Coordinator (CRC) to join our team. This is a fully onsite role and is open only to candidates local to Honolulu, HI (96813).We are specifically seeking candidates with hands-on Clinical Research Coordinator experience in physician office or private practice clinical trial settings. Experience gained exclusively in hospital or university-based research environments does not fully align with the workflow and operational structure of this position.Key Responsibilities:Lead the coordination and execution of clinical trials across all phases: start-up, enrollment, maintenance, and close-out.Ensure proper receipt, handling, and accountability of investigational product (IP).Conduct and document the informed consent process in compliance with protocols and regulations.Serve as a liaison between physicians, study sponsors, and internal team members.Achieve or exceed study enrollment targets at assigned sites.Complete accurate and timely data entry in electronic data capture systems.Resolve data queries promptly to support project timelines and database lock.Maintain compliance with GCP, company SOPs, and industry regulations.Qualifications:2-5 years of Clinical Research Coordinator experience in a physician practice or private research setting.Strong understanding of investigational product (IP) receipt, handling, and accountability.Proven experience conducting the informed consent process.Demonstrated ability to independently coordinate and manage clinical trials.Excellent organizational, communication, and problem-solving skills.Must be local to the area (onsite only; no relocation or remote work).Requirements added by the job posterAuthorized to work in the United States