Clinical Research Associate
ICON · TX +1 more
Clinical OperationsFull-timeCompany career page
The apply link worked recently (not employer-confirmed).
Role summary
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.
What they're looking for
- 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
What you'll be doing
- 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
CompensationCompetitive base salary and performance related incentives
Privacy & handoff
This role links to ICON's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.