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CDC II

ICON · Taipei, Taiwan

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Role summary

Clinical Data Coordinator II role at a global clinical research organization supporting pharmaceutical trials. Design and analyze clinical trial data, manage eCRF systems, and coordinate data validation and reconciliation activities in a sponsor-dedicated team 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 environment
  • 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 clinical and third-party data reconciliation based on edit specifications
  • Track and communicate study and task metrics to data scientist and project teams
  • Address data-related questions and recommend solutions
  • Identify root causes and systematically resolve data issues

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