Responsibilities;
-Clinical data collection, cleaning and analysis
-Provide supervision and guidance to CROs, ensuring timely delivery and compliance
-Oversee CRO data management and function
-Responsible for research start-up to the database lock for the EDC
-Ensure compliance with SOPs, GCP and ICH guidelines
Requirements;
-BSc in Science subject with relevant experience as a CDM in a CRO, pharma, or biotech
-Knowledge of industry and regulatory guidelines
-Fluent in Chinese and/or Mandarin
