Clinical Research Coordinator

National Institute of Clinical Research, Inc.; Torrance (CA); On-site; USD 60,000 - 90,000; Full time

Benefits offered by this job

Medical Insurance

Dental Insurance

Vision Insurance

401(k) with company match

Paid Time Off

Job summary

The National Institute of Clinical Research, Inc. is seeking a Clinical Research Coordinator (CRC) to oversee studies from initiation through final report. This onsite role is based in Torrance, CA and requires attention to quality, compliance, and efficient trial conduct.

You will manage study activities, coordinate visits, ensure data integrity, and maintain GCP/ICH compliance, collaborating with investigators, sponsors, and staff to drive trial success. Bilingual English/Spanish is a plus.

Qualifications

• Minimum 2 years clinical research experience.
• In-depth knowledge of GCP and ICH guidelines.
• Strong interpersonal and planning abilities with attention to detail.
• Willingness to travel to site locations (Hesperia and Barstow).
• Bilingual in English/Spanish is 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 GCP and ICH guidelines.
• Coordinate study visits, track enrollment, and ensure documentation.
• Collaborate with investigators, sponsors, and clinical staff to support trial success.

Skills

GCP knowledge

Communication skills

Organizational skills

Troubleshooting

Job description

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 Torrance, 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)