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Full-Time Opportunity: This is a permanent, full-time position with a competitive package and real career growth potential.
Job Description
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...