Clinical Research Coordinator

National Institute of Clinical Research, Inc.•Garden Grove, CA

8h•$23 - $32•Onsite

About The Position

The Clinical Research Coordinator (CRC) manages clinical studies from initiation through completion of the final study report, ensuring quality, compliance, and efficiency in clinical trial conduct. The position oversees daily trial operations, protocol adherence, data integrity, regulatory compliance, study visits, enrollment, and documentation. The CRC also anticipates study needs, resolves issues, and collaborates with investigators, sponsors, and clinical staff. This is a full-time, onsite position for someone local to the Orange County, California area; travel to other sites is required as needed.

Requirements

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.
Skill in troubleshooting and conflict resolution.
Must be local to the Orange County, California area.
Travel to other sites as required.

Nice To Haves

Minimum of 2 years of clinical research experience.
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 through troubleshooting and conflict-resolution skills.
Collaborate with investigators, sponsors, and clinical staff to support trial success.
Travel to other sites as required.