Join ICON plc, a world-leading healthcare intelligence organization, as a Clinical Research Associate (CRA) in China. In this field-based role, you will be the critical link between ICON and our clinical trial sites, ensuring the successful execution and monitoring of groundbreaking clinical studies. Your work will directly contribute to advancing medical treatments and improving patient lives.
Your Key Responsibilities
Site Management & Monitoring
- Conduct site qualification, initiation, monitoring, and close-out visits for clinical trials across China.
- Ensure site compliance with protocols, ICH-GCP guidelines, and regulatory requirements.
- Perform source data verification and resolve data queries to maintain high-quality clinical data.
Study Coordination & Documentation
- Coordinate all study start-up and monitoring activities, maintaining accurate study documentation.
- Prepare and review essential study documents, including reports and feasibility studies.
- Manage study costs efficiently and respond to sponsor queries in a timely manner.
Stakeholder Collaboration & Patient Safety
- Build and maintain strong, collaborative relationships with clinical investigators and site staff.
- Serve as the primary point of contact for sites, addressing queries and ensuring smooth study conduct.
- Uphold the highest standards of patient safety through rigorous compliance with protocols.
Your Profile: Skills & Experience
Essential Qualifications
- University degree in Medicine, Life Sciences, or a related field.
- Knowledge of ICH-GCP guidelines and experience in reviewing medical data.
- Excellent written and verbal communication skills in English and Mandarin.
- Willingness and ability to travel at least 60% of the time (domestic & international).
- Valid driver's license.
Key Skills & Attributes
- Strong interpersonal skills to build rapport with site staff and investigators.
- Proactive problem-solving abilities and attention to detail.
- Ability to work independently and manage multiple priorities effectively.
Why Join ICON?
Our success depends on our people. When you join ICON, you become part of a team that values your contribution.
- Impactful Work: Play a direct role in bringing new medical treatments to patients in China.
- Career Growth: Clear paths for professional development in a global CRO.
- Competitive Benefits: A comprehensive package including health insurance, retirement planning, and generous leave.
- Supportive Environment: Access to a global employee assistance program and a diverse, inclusive culture.
Ready to Advance Clinical Research in China?
If you are a clinical research professional with a passion for excellence and a drive to make a difference, we encourage you to apply.
