Knowledge and Experience:
• Demonstrates technical aptitude with awareness/potential prior experience in Microsoft Office Products (basic computer skills).
• Basic understanding of data management processes and data validation flow (e.g. Data cleaning, DB lock)
• Basic understanding of relevant ICH-GCP Guidelines, local regulatory requirements and Parexel SOPs and study specific procedures
• Basic knowledge of Clinical Data Management Systems (e.g. InForm, Rave, Veeva, Datalabs, ClinBase.)
• Basic understanding of Clinical Study Team roles within Data Management
• Experience in clinical research industry
• Basic knowledge of medical terminology and coding dictionaries (e.g. MedDRA & WHODRUG)
• Basic knowledge of Data Management Operational processes and tasks during study start-up, conduct and close-out
• Basic knowledge of Database set-up activities, including but not limited to Database Configuration Specifications and setup of Data Validation.
Education:
• Bachelor’s degree and/or other medical qualifications or relevant industry experience.
