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Clinical Research Associate
1 month ago
Clinical Research Associate
Working Model: Hong Kong Client Office based
As a Clinical Research Associate, you will be joining the world's largest & most comprehensive clinical research organization, powered by healthcare intelligence.
What you will be doing:
- Site Monitoring
- Site Management
- Ultimately responsible for the successful management of investigator sites throughout the site lifecycle
- Working in accordance with ICH-GCP guidelines, the study protocol, applicable local and international regulatory requirements and internal Standard Operating Procedures
You are:
- Bachelor's degree or above
- More than 1 year of global oncology study experience as a CRA
- More than 1 year of site monitoring experience
- Good at English reading and writing; proficiency in Cantonese and Chinese
Why ICON?
Our focus is to provide you with a comprehensive and competitive total reward package that comprises not only an excellent level of base pay but also a wide range of variable pay and recognition programs. In addition, our best-in-class employee benefits, supportive policies, and wellbeing initiatives are tailored to support you and your family at all stages of your career - both now and into the future.
Our success depends on the knowledge, capabilities, and quality of our people. That's why we are committed to developing our employees in a continuous learning culture – one where we challenge you with engaging work and where every experience adds to your professional development.
ICON, including subsidiaries, is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.
