Aufgaben

  • Oversee data management activities to ensure compliance with regulations and company procedures
  • Support the design, development, and testing of (e)CRFs and data review tools
  • Contribute to data management documentation and reporting
  • Conduct data review, manage discrepancies and queries, and track protocol deviations
  • Assist in database lock activities and provide project metrics
  • Archive study documentation according to applicable guidelines

Qualifikationen

  • Bachelor’s degree or higher in a pharmaceutical, biomedical, or related scientific discipline
  • At least 2 years of experience in Clinical Research or Clinical Data Management in the pharmaceutical or biotech industry
  • Strong understanding of clinical trial databases, data flow, and (e)CRF design
  • Knowledge of ICH-GCP and international clinical research regulations
  • Excellent organizational and teamwork skills
  • Fluency in written and spoken English