Clinical Research Coordinator

Our take on this role

About this role

Manage Phase I–IV clinical studies from placement through closeout, overseeing trial protocols, data accuracy, and study visits. This is a full-time onsite role requiring travel to additional sites in Hesperia and Barstow.

What could you bring from clinical work?

• Nurses and PTs: Following clinical protocols and maintaining accurate patient records could help you oversee trial protocol adherence and data integrity.
• OTs and SLPs: Your experience coordinating assessment visits and documenting outcomes may help with organizing study visits and maintaining accurate study records.
• Social workers: If you've coordinated work across interdisciplinary clinical teams, that experience could help you collaborate with investigators 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 required to additional site locations in Hesperia and Barstow.

Must be local to San Antonio, TX 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)