Clinical Research Associate
Icon Clinical Research
Clinical Research Associate II position at ICON supporting sponsor-dedicated cardiology and obesity trials. Responsibilities include site monitoring, protocol compliance oversight, and clinical data quality assurance across the trial lifecycle.
Responsibilities
- Conduct site qualification, initiation, monitoring, and closeout visits for clinical trials
- Ensure protocol compliance, data integrity, and patient safety throughout trial process
- Collaborate with investigators and site staff to facilitate 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 Clinical Research Associate experience
- In-depth knowledge of clinical trial processes, ICH-GCP guidelines, and regulations
- Strong organizational and communication skills with attention to detail
- Ability to work independently and collaboratively in fast-paced environments
- Willingness to travel approximately 60% as required
Compensation: Competitive base salary and performance related incentives
Vacancy posted 4 days ago
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