Job Details

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 poster

• Authorized to work in the United States