> Markdown version of [/jobs/ext/3195468-clinic-information-processing-coordinator](https://www.wearedevelopers.com/jobs/ext/3195468-clinic-information-processing-coordinator). Every page supports `.md` or `Accept: text/markdown`. Links point to the HTML versions so they work for humans too. Agent guide: [/agents.md](https://www.wearedevelopers.com/agents.md). --- # Clinic Information Processing Coordinator - **Company:** DRAFTHIRE LLC - **Location:** Walnut Creek, CA, United States - **Experience:** Starter - **Salary:** $52,000.0 - $60,320.0 - **Contract:** Permanent contract - **Skills:** Data Systems, Microsoft Office, Web Applications, Data Processing - **Published:** September 17, 2026 - **Apply:** https://www.indeed.com/viewjob?jk=53f27eb54b3c44cf ## About the Role * 1-3+ years of experience in clinical research, biological research, or a closely related environment * Bachelor's degree preferred, although relevant professional experience may be considered in place of a degree * Working knowledge of clinical research processes, medical terminology, and industry standards * Strong attention to detail with the ability to identify discrepancies and work through data or documentation issues * Comfortable using Microsoft Office and web-based research or data systems * Organized, dependable, and able to work both independently and collaboratively in a fast-paced research environment ## Description Our client is seeking a Clinic Information Processing Coordinator to support the accuracy, completeness, and organization of clinical research information at its Walnut Creek location. This is a strong opportunity for someone with clinical research experience who enjoys detail-oriented, non-patient-facing work involving study documentation, data entry, quality review, and problem solving., * Review cproblem-solvingh records for completeness, accuracy, and consistency with study protocols, internal procedures, and research guidelines * Enter study information into electronic case report form systems accurately and within required timelines * Identify missing, inconsistent, or questionable information and work with research staff to resolve issues * Review and respond to data queries while helping ensure information matches supporting source documentation * Support sponsor and monitor visits by helping address outstanding documentation and data questions * Partner with coordinators, quality team members, and other research staff to maintain accurate and organized study records