Clinical Research Associate
2 days ago
About ICON
ICON is a world-leading healthcare intelligence and clinical research organization that fosters an inclusive environment driving innovation and excellence.
We welcome talented professionals to join our mission to shape the future of clinical development.
What We Offer
In addition to your competitive salary, you will receive a range of benefits designed to support your well-being and work-life balance, including various annual leave entitlements, health insurance options, retirement planning opportunities, and more.
As a Clinical Research Associate with ICON, you will have the opportunity to work on multiple Phase II and III clinical trial sites across different therapeutic areas.
Your Responsibilities
- Monitor multiple Phase II and III clinical trial sites to ensure compliance with ICH/GCP guidelines.
- Assist other CRAs with co-monitoring activities, both remote and on-site.
- Utilize your customer service mindset to deliver value, build loyalty, and trust with investigators and study coordinators.
- Collaborate with the team to develop commitment to study timelines and objectives through regular visits with site staff.
- Ensure patient safety and data integrity by reviewing source documents and electronic case report forms (eCRFs).
- Educate site staff on GCP/ICH practices and ensure adherence to quality standards.
Requirements
- Bachelor's Degree (or equivalent) with 2-4 years of relevant healthcare experience in the pharma or clinical research industry.
- Minimum 2 years of monitoring and site management experience.
- Scientific background and proficiency in medical terminology.
- Working knowledge of local regulations and demonstrated expertise in ICH/GCP guidelines.
- Excellent record-keeping skills and attention to detail.
- Experience conducting site selection, initiation, routine monitoring, and close-out visits.
Competitive Salary: $80,000 - $110,000 per annum, depending on location and experience.
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