Clinical Research Associate
ICON · Auckland, New Zealand
Clinical OperationsFull-timeCompany career page
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Role summary
ICON seeks a Clinical Research Associate II/Senior to monitor clinical trials, ensure protocol compliance, and maintain data integrity. The role involves site management, stakeholder collaboration, and documentation review to support the development of new medicines and treatments.
What they're looking for
- Bachelor's degree in scientific or healthcare-related field
- Minimum 2 years 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
What you'll be doing
- 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
- Perform data review and resolve queries to maintain high-quality clinical data
- Prepare and review study documentation including protocols and clinical study reports
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.