Ihre Aufgaben

• Regulatory & Internal Compliance: Guarantees that all clinical data management and biometry tasks for the designated study comply with internal innovation standards and applicable regulatory requirements
• Milestone Delivery: Achieves all study timelines and milestones regarding data management outputs and deliverables
• Data Consistency: Maintains uniform data handling, processing, and validation methods across all allocated clinical trials
• Project Leadership: Directs, leads, and oversees end-to-end data management workflows for the specified study
• Protocol Input: Contributes critical data management expertise and insights during the drafting and design phase of the study protocol
• eCRF Setup: Coordinates and manages the creation, design, and setup of the electronic Case Report Form (eCRF) according to company standards
• Technical Documentation: Authors comprehensive data management documentation...