Clinical Research Coordinator

National Institute of Clinical Research; Torrance (CA); On-site; USD 60,000 - 80,000; Full time

Benefits offered by this job

Medical, Dental, and Vision Insurance

401(k) with company match

Paid Time Off (PTO)

Job summary

The National Institute of Clinical Research (NICR) is seeking a Clinical Research Coordinator to manage studies from initiation through final report. This onsite role requires meticulous compliance with GCP/ICH and strong data integrity skills.

Local to Torrance, CA, travel to Hesperia and Barstow is required; bilingual English/Spanish is a plus. Primary duties include coordinating visits, tracking enrollment, and ensuring study documentation is accurate and complete.

Qualifications

• Minimum of 2 years of clinical research experience.
• Knowledge of GCP and ICH guidelines.
• Strong communication and organizational skills.
• Ability to travel to additional site locations as needed.
• Local to the Torrance, CA area.

Responsibilities

• Manage clinical studies from initiation through 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 document accurately.
• Anticipate study needs and coordinate proactively.
• Resolve issues through troubleshooting and conflict-resolution.

Skills

GCP & ICH knowledge

Data integrity

Interpersonal skills

Organizational skills

Planning abilities

Troubleshooting

Conflict resolution

Bilingual English/Spanish (plus)

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)