Clinical Research Associate
$91.34k - $114.17kICON
Clinical Research Associate position in oncology for ICON's sponsor-dedicated model, based in Ohio, Pennsylvania, or Virginia. The role involves clinical trial monitoring, site management, protocol compliance oversight, and data quality assurance across multiple study sites.
Responsibilities
- Conduct site qualification, initiation, monitoring, and close-out visits
- Ensure protocol compliance, data integrity, and patient safety throughout trials
- Collaborate with investigators and site staff on study conduct
- Review data and resolve queries to maintain high-quality clinical information
- Prepare and review study documentation including protocols and clinical reports
Requirements
- Bachelor's degree in scientific or healthcare-related field
- Minimum 2 years experience as Clinical Research Associate
- Oncology monitoring experience required
- In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines
- Strong organizational and communication skills with attention to detail
- Ability to travel 60-75% within region as required
- Legal right to work in the United States
Compensation: $91,336-$114,170 base
Vacancy posted 15 days ago
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