Clinical Research Coordinator

National Institute•Torrance, CA

25d•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, coordinates study visits and enrollment, maintains accurate documentation, and works with investigators, sponsors, and clinical staff to support successful trials. The role is full-time and onsite in the Torrance, California area; it is not remote or hybrid. Travel to additional site locations in Hesperia and Barstow is required. Bilingual English/Spanish skills are a plus.

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.
Troubleshooting and conflict-resolution skills.
Must be local to the Torrance, California area.
Travel to additional site locations in Hesperia and Barstow is required.

Nice To Haves

A minimum of 2 years of clinical research experience is preferred.
Bilingual English/Spanish skills are a plus.

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.