Onsite Clinical Research Coordinator - Torrance

National Institute of Clinical Research

Torrance (CA)

On-site

USD 60,000 - 80,000

Full time

27 hours ago
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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 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.

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