CRA
$91.34k - $114.17kICON
Clinical Research Associate II position at ICON involving clinical trial monitoring, data integrity management, and regulatory compliance. Role is based in Sherman Oaks, CA with approximately 60% travel requirement and operates within a sponsor-dedicated model.
Responsibilities
- Conduct site qualification, initiation, monitoring, and close-out visits for clinical trials
- Ensure protocol compliance, data integrity, and patient safety throughout trial process
- Collaborate with investigators and site staff to facilitate smooth study conduct
- Perform data review and resolve queries to maintain high-quality clinical data
- Contribute to preparation and review of study documentation including protocols and reports
Requirements
- Bachelor's degree in scientific or healthcare-related field
- Minimum 2 years of experience as a Clinical Research Associate
- In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines
- Strong organizational and communication skills with attention to detail
- Ability to work independently and collaboratively in fast-paced environment
- Willingness to travel approximately 60% as required
- Legal right to work in the United States
Compensation: $91,336.00-$114,170.00 base
Vacancy posted 19 days ago
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