
Clinical Study Coordinator
- Duarte, CA
- $41.92-64.97 per hour
- Permanent
- Full-time
- Understand and apply federal regulations (FDA, OHRP, GCP/ICH, HIPAA) and institutional policies.
- Follow and execute clinical trial protocols and procedures.
- Coordinate participant recruitment, informed consent, and care.
- Communicate with participants, investigators, and sponsors to ensure clear understanding and compliance.
- Monitor and document participant eligibility, safety, and protocol adherence, and report adverse events promptly.
- Pursue continuous education and training opportunities, staying updated with the latest clinical research information, and maintain necessary certifications and licensure.
- Bachelor's degree in Science, Health or related field from an accredited university; 3 additional years of experience plus the minimum experience requirement may substitute for minimum education.
- Minimum of 2 years research or relevant clinical experience
- ACRP or SOCRA certification within 1 year of employment
- International Air Transport Association (IATA) within 1 month of employment
- Good Clinical Practice (GCP) within 1 month of employment
- Human Subjects Protection (HSP) within 1 month of employment
- Basic Life Support (BLS) within 1 month of employment