Launch your clinical monitoring career with a structured development program. ICON is seeking an In-House CRA to join our Beijing office as part of our world-class training program. This role is designed for clinical research professionals with 1+ years of experience, offering a clear pathway to advance into a traveling CRA position while performing essential remote site management activities for global clinical trials.
Key Responsibilities
You will serve as the primary in-house contact for clinical sites, building the foundational skills required for a successful monitoring career.
Remote Site Management & Support:
- Serve as the primary in-house contact for investigators and sites, conducting remote site management activities according to the Study Monitoring Plan.
- Contact clinical sites for specific requests including enrolment updates, missing documentation, data query follow-up, and action item resolution.
- Maintain timelines and ensure the accuracy and completeness of data entered into ICON systems.
Compliance & Collaboration:
- Become familiar with ICON SOPs, ICH GCP guidelines, and applicable regulations.
- Maintain professional relationships with the study team, sites, and sponsors.
- Participate in project and departmental meetings, contributing to team goals and process improvements.
Your Profile
Essential Qualifications:
- Minimum Bachelor's degree in a Life Science or related field.
- At least 12 months of experience as a Clinical Trial Assistant (CTA) or in a similar role within the clinical/pharmaceutical industry.
- Understanding of ICH GCP compliance and clinical research principles.
Required Skills:
- Excellent communication and organizational skills.
- A proactive, team-oriented mindset with strong attention to detail.
- Willingness to travel as needed for role development.
Why Join ICON?
This is more than a job—it's a launchpad for your career. ICON's award-winning development program provides:
- Structured Career Growth: A defined path to advance into a traveling CRA role.
- Competitive Salary & Benefits: Comprehensive package including health insurance and retirement planning.
- Global Impact: Contribute to studies that have led to the approval of 18 of the world's top 20 drugs.
- Supportive Environment: A culture that rewards high performance and nurtures talent.
Ready to fast-track your clinical research career? We encourage you to apply even if you don't meet every single requirement. Your potential is what we value most.
