Clinical Research Coordinator
National Institute of Clinical ResearchBakersfield, California, United States
Posted December 17, 2025
Full Time
About the Company
The National Institute of Clinical Research (NICR) is a physician‑owned, multi‑site Clinical Trial Management Organization dedicated to delivering high‑quality, efficient clinical trials. Leveraging state‑of‑the‑art medical capabilities, NICR manages studies across all phases—from Phase 1 through Phase 4—ensuring rigorous scientific standards and regulatory compliance. Its independent structure allows tailored, patient‑centric solutions that accelerate development timelines while maintaining uncompromised safety and data integrity. By combining clinical expertise with operational excellence, NICR distinguishes itself as a trusted partner for sponsors seeking reliable, scalable trial execution.
Job Description
The National Institute of Clinical Research (NICR) is an independent, multi-site Site Management Organization (SMO) conducting Phase I–IV clinical trials since 1996. With over 500 successful trials completed, we are dedicated to delivering the highest quality in clinical research. The Clinical Research Coordinator (CRC) will play a key role in managing studies from initiation through completion of the final study report.
Requirements
- Manage clinical studies from placement through study closeout.
- Oversee daily trial operations to ensure protocol adherence and data integrity.
- Maintain regulatory compliance with Good Clinical Practice (GCP) and ICH guidelines.
- Coordinate study visits, track enrollment, and ensure accurate documentation.
- Anticipate and coordinate study needs proactively.
- Resolve issues through strong troubleshooting and conflict-resolution skills.
- Collaborate with investigators, sponsors, and clinical staff to support trial success.
Benefits
- Medical, Dental, and Vision Insurance
- 401(k) with company match
- Paid Time Off (PTO)