Clinical Trial Study Coordinator
$56,160–$64,480 year
On-siteChico, California, United States
Job Summary
Conduct participant screening, recruitment, and enrollment by guiding individuals through informed consent and performing required protocol testing. Coordinate study visits for screening, follow-ups, and lab appointments while collecting, entering, and maintaining high-accuracy study data. Monitor participant adherence, report adverse events, and administer outcome questionnaires. Execute study protocols consistently, dispense investigational products, and record vital signs as needed. Maintain regulatory binders, participant records, and accurate documentation while ensuring compliance with ICH-GCP, FDA regulations, and institutional policies. Communicate timely with sponsors, CROs, and the research team. Participate in investigator and study team meetings as directed.
Required Qualifications
- Strong understanding of clinical research practices and regulatory guidelines (e.g., ICH-GCP)
- Familiarity with clinical trial documentation and data management systems
- Knowledge of medical terminology and human subject research ethics
- Excellent interpersonal and communication skills
- Highly organized with strong attention to detail
- Effective time management and problem-solving skills
- Ability to work independently and collaboratively in a fast-paced environment
- Proficiency in Microsoft Office Suite and electronic data capture systems
- Flexibility and adaptability to shifting priorities
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