Senior CDC
On-site · Shanghai, Shanghai, China or Hangzhou, Zhejiang, China
Job Summary
Senior CDC at ICON leads on clinical research tasks with a focus on data management and quality, designing and analysing clinical trials, developing data management strategies, mentoring junior data coordinators, and ensuring study timelines. Responsibilities include creating data management plans, resolving data discrepancies, collaborating with clinical operations and biostatistics, filing and archiving study documentation, and dispatching queries to investigator sites. Requirements include a Bachelor’s degree in Life Sciences or Healthcare, proven clinical data management experience, familiarity with data management software (e.g., Medidata, Oracle RDC), attention to detail, strong communication, and knowledge of regulatory guidelines (ICH-GCP) with willingness to travel ~5%, and legal right to work. ICON emphasizes equal opportunity and a comprehensive rewards package.
Required Qualifications
- Bachelor's degree in Life Sciences or Healthcare
- Proven experience in clinical data management within the pharmaceutical or biotechnology industry
- Familiarity with data management software and systems (e.g., Medidata, Oracle RDC, or similar)
- Strong attention to detail
- Excellent communication skills
- Knowledge of regulatory guidelines and standards (e.g., ICH-GCP) is a plus
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