Clinical Research Coordinator

National Institute of Clinical Research; Garden Grove (CA); On-site; USD 70,000 - 95,000; 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) seeks a Clinical Research Coordinator to manage studies from initiation through closeout on site in Orange County, CA, ensuring quality, compliance, and efficient trial conduct under GCP and ICH guidelines.

Requirements: minimum 2 years clinical research experience; strong communication, organization, and problem-solving skills; willingness to travel; bilingual English/Spanish is a plus; full-time onsite position.

Qualifications

• Minimum of 2 years in clinical research.
• Knowledge of GCP and ICH guidelines.
• Strong interpersonal and communication skills.
• Excellent organizational and planning abilities with attention to detail.
• Ability to anticipate study needs and coordinate effectively.
• Proficient troubleshooting and conflict resolution.
• Willingness to travel to other sites.

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 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.

Skills

Clinical research experience

GCP knowledge

Interpersonal communication

Organizational skills

Study coordination

Troubleshooting

Bilingual (Eng/Span) close to required

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 to other sites as required.

Must be local to Orange County, 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)