Clinical Research Associate II/ Senior Clinical Research Associate
$80,000–$100,000 year
On-site · Hong Kong, Hong Kong
Job Summary
As a Senior Clinical Research Associate (CRA) at ICON Plc, you will oversee and manage clinical trial activities ensuring adherence to regulatory requirements and Good Clinical Practice (GCP) standards. Responsibilities include monitoring clinical trial sites, conducting site visits, collaborating with cross-functional teams, and providing training to site staff and other CRAs. Candidates should possess an advanced degree in a relevant field, extensive experience in clinical research, and strong organizational skills.
Required Qualifications
- Extensive experience as a Clinical Research Associate
- Strong understanding of clinical trial processes and regulatory requirements
- Expertise in monitoring practices, data integrity, and site management
Desired Qualifications
- Strong organizational and problem-solving skills
- Proficiency in relevant clinical trial software and tools
- Excellent communication and interpersonal skills
- Ability to manage multiple sites and projects simultaneously
Additional Requirements
- Ability to travel internationally and domestically
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