* Salary estimates based on industry data for similar roles
Accelerate clinical development with a global industry leader. ICON is seeking an experienced Clinical Research Associate II (CRA II) to join our team in Hong Kong. In this client-embedded role, you will be pivotal in managing site activities, ensuring data integrity, and upholding patient safety across cutting-edge clinical trials. This position offers a unique blend of autonomy and collaboration, with a flexible work model and the opportunity to make a tangible impact on global health.
Key Responsibilities
You will be the primary point of contact for clinical trial sites, managing the end-to-end monitoring process to ensure successful study delivery.
Site Management & Monitoring:
- Conduct all types of monitoring visits—from site qualification, initiation, and monitoring to close-out—ensuring adherence to protocol and regulations.
- Collaborate directly with investigators and site staff to build strong relationships and facilitate smooth study conduct.
- Perform source data verification (SDV), review case report forms (eCRFs), and resolve data queries to maintain the highest standards of data quality.
Compliance & Documentation:
- Ensure all site activities comply with ICH-GCP guidelines, local regulations, and study protocols.
- Contribute to the preparation and review of essential study documents, including protocols, informed consent forms, and clinical study reports.
- Proactively identify and manage site-related issues, ensuring patient safety and data integrity are never compromised.
Your Profile
Essential Qualifications:
- Bachelor’s degree in a Life Science, Nursing, or a related healthcare field.
- Minimum of 2 years of experience as a Clinical Research Associate (CRA) with independent monitoring experience.
- In-depth knowledge of clinical trial processes and ICH-GCP guidelines.
- Strong organizational skills and meticulous attention to detail.
Logistics & Skills:
- Ability to travel approximately 60% of the time (domestically and internationally) and a valid driver’s license.
- Excellent communication and interpersonal skills, with the ability to work both independently and as part of a global team.
- Proactive problem-solver who thrives in a fast-paced, dynamic environment.
Why Join ICON?
Our success depends on our people. When you join ICON, you become part of a team dedicated to excellence and innovation in clinical development. We offer:
- Competitive salary and a comprehensive benefits package focused on well-being.
- Flexible working model (client office-based with WFH flexibility).
- Health insurance and competitive retirement planning.
- Global Employee Assistance Programme and extensive well-being support.
- A diverse, inclusive culture that rewards high performance and nurtures talent.
Ready to shape the future of clinical development? We encourage you to apply even if you don't meet every single requirement. Your unique skills could be exactly what we're looking for.
