Clinical Research Coordinator

Our take on this role

About this role

Manage Phase I–IV clinical studies from placement through closeout, overseeing protocol adherence, data integrity, and study visits. This is a full-time onsite role requiring Orange County, CA residency and travel to other sites as required.

What could you bring from clinical work?

• Nurses and PTs: Following clinical protocols and maintaining accurate patient records could help you monitor trial protocol adherence and data integrity.
• OTs and SLPs: Your experience coordinating assessment visits and maintaining structured clinical documentation may help with arranging study visits and keeping accurate study records.
• Social workers: Coordinating across clinical teams to resolve service-delivery issues could help you collaborate with investigators, sponsors, and clinical staff.

Full job description from National Institute of Clinical Research, Inc.

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.

Position Summary

The Clinical Research Coordinator (CRC) will play a key role in managing studies from initiation through completion of the final study report. The CRC is responsible for ensuring quality, compliance, and efficiency in the conduct of clinical trials.

Key Responsibilities

• 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.

Bilingual in English/Spanish is a plus!

Requirements

• Preferred: Minimum of 2 years of clinical research experience.
• In-depth knowledge of clinical trial processes, GCP, and ICH guidelines.
• Strong interpersonal and communication skills.
• Exceptional organizational and planning abilities with strong attention to detail.
• Proven ability to anticipate study needs and coordinate effectively.
• Skilled in troubleshooting and conflict resolution.
• Travel to other sites as required.

Must be local to Orange County, CA area – Full-time Onsite /this is not a remote or hybrid position

Benefits

• Medical, Dental, and Vision Insurance
• 401(k) with company match
• Paid Time Off (PTO)