Senior CRC — CNS Trials Lead Irvine

Irvine Clinical Research; Los Angeles (CA); On-site; USD 77,000 - 94,000; Full time

Benefits offered by this job

Health insurance

Paid time off (3 weeks)

Job summary

Inglewood Clinical Research in Irvine is seeking a Senior Clinical Research Coordinator with extensive trial experience to serve as the primary coordinator on Phase I–III studies in Neurology, Psychiatry, and Cardiometabolic. The candidate will lead start-up, execution, and documentation activities while ensuring GCP compliance.

Responsibilities include coordinating day-to-day operations, conducting procedures per protocol, and maintaining data in CTMS and paper files.

Qualifications

• 5+ years of industry-sponsored drug trials experience.
• Experience in Phase II/III trials and high enrollment.
• Strong attention to detail and ability to multitask.
• Proficiency in CTMS and study documentation.
• Excellent English communication skills.

Responsibilities

• Coordinate day-to-day operations of clinical studies.
• Perform study procedures per GCP and protocols.
• Maintain paper and electronic study data accurately.
• Collaborate with recruitment to meet enrollment goals.
• Mentor coordinators and lead team on productivity and quality.

Skills

Clinical research coordination

CTMS experience

Leadership

Attention to detail

English proficiency

Tools

CTMS

Job description

Inglewood Clinical Research in Irvine is seeking a Senior Clinical Research Coordinator with extensive trial experience to serve as the primary coordinator on Phase I–III studies in Neurology, Psychiatry, and Cardiometabolic. The candidate will lead start-up, execution, and documentation activities while ensuring GCP compliance.

Responsibilities include coordinating day-to-day operations, conducting procedures per protocol, and maintaining data in CTMS and paper files.