Clinical Research Coordinator

National Institute•Garden Grove, CA

18d•Onsite

About The Position

The Clinical Research Coordinator (CRC) manages clinical studies from initiation through completion of the final study report and closeout. The role supports quality, compliance, and efficiency in clinical trial conduct by overseeing daily operations, coordinating study visits and enrollment, maintaining accurate documentation, and ensuring protocol adherence and data integrity. The CRC works with investigators, sponsors, and clinical staff, anticipates study needs, and addresses issues through troubleshooting and conflict resolution. The position is full-time and onsite in the Orange County, California area; it is not remote or hybrid. Travel to other sites may be required. Bilingual English/Spanish skills are a plus. Compensation is $23.00–$32.00 per hour.

Requirements

Minimum of 2 years of clinical research experience is preferred.
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.
Ability to anticipate study needs and coordinate effectively.
Skills in troubleshooting and conflict resolution.
Must be local to the Orange County, California area.

Nice To Haves

Bilingual in English and Spanish.

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 using troubleshooting and conflict-resolution skills.
Collaborate with investigators, sponsors, and clinical staff to support trial success.
Travel to other sites as required.