CDC II
ICON · Taipei, Taiwan
Clinical OperationsFull-timeCompany career page
The apply link worked recently (not employer-confirmed).
Role summary
Clinical Data Coordinator II role at a leading contract research organization, supporting sponsor-dedicated clinical trial operations. The position involves designing and analyzing clinical trial data, managing eCRF systems, and ensuring data quality and regulatory compliance in a collaborative, fast-paced environment.
What they're looking for
- Bachelor's degree in Life Sciences, Healthcare, or related field
- Intermediate clinical data management experience in pharmaceutical or biotechnology
- Proficiency with data management software such as Medidata or Oracle RDC
- Strong attention to detail and ability to work in fast-paced settings
- Excellent cross-functional communication and collaboration skills
- Knowledge of ICH-GCP regulatory guidelines preferred
What you'll be doing
- Assist Data Management Study Lead with eCRF maintenance and data validation specifications
- Manage reconciliation of clinical and third-party data according to edit specifications
- Track and communicate study and task metrics to data scientists and project teams
- Address data-related inquiries and recommend potential solutions
- Identify root causes and systematically resolve data issues
Privacy & handoff
This role links to ICON's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.