Clinical Trial Associate
Clinical Careers Page(1 month ago)
About this role
A Clinical Trial Administrator at ICON in Beijing supports the company’s clinical research mission within an office-based role. The position is part of a global clinical research organization focused on advancing innovative treatments and therapies. The role is suited to candidates with a scientific or healthcare bachelor’s degree and interest in clinical research.
Required Skills
- Clinical Trials
- Regulatory Compliance
- Document Management
- Study Coordination
- Informed Consent
- CRF Preparation
- Communication
- Detail Orientation
Qualifications
- Bachelor's Degree in Scientific or Healthcare Field
About Clinical Careers Page
iconplc.comICON plc is a global clinical research organisation (CRO) that provides outsourced clinical development and commercialisation services to pharmaceutical, biotechnology and medical device companies. It offers end-to-end drug and device development support — including clinical trial management across phases, data management and biostatistics, regulatory and safety/pharmacovigilance, and commercialisation and market-access services. ICON combines scientific and therapeutic expertise with technology and a scalable global operations network to accelerate development and bring therapies to patients. Clients engage ICON for integrated, experienced CRO support across the full product lifecycle.
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