Clinical Research Coordinator

Clinical Research Coordinator

Garden Grove, California





Summary:

The CRC is responsible for managing clinical studies from initiation to completion, ensuring quality, compliance, and efficiency throughout the clinical trial process.





Responsibilities:


- Oversee all phases of clinical studies, ensuring smooth progression from start to finish.
- Supervise daily operations of clinical trials, maintaining strict adherence to study protocols and data accuracy.
- Ensure compliance with regulatory standards, including Good Clinical Practice (GCP) and ICH guidelines.
- Coordinate and document study visits, monitor participant enrollment, and maintain accurate records.
- Proactively identify and address study requirements to support successful trial execution.
- Utilize strong troubleshooting and conflict-resolution skills to resolve study-related issues.
- Work collaboratively with investigators, sponsors, and clinical staff to achieve study objectives.
- Maintain high standards of organization, planning, and attention to detail throughout all study activities.






Qualifications:


- Minimum of 2 years of clinical research experience preferred.
- Comprehensive understanding of clinical trial processes, GCP, and ICH guidelines.
- Excellent interpersonal and communication skills.
- Strong organizational and planning abilities with keen attention to detail.
- Demonstrated ability to anticipate study needs and coordinate effectively.
- Proficient in troubleshooting and conflict resolution.
- Bilingual in English/Spanish preferred.