13 days ago
Remote, BulgariaMid Level
Responsibilities
- Create EDC systems for complex projects, including structure, workflows, edit checks, and user roles and permissions.
- Configure applicable functionality such as randomization, ePRO, IMP management, targeted SDV, and other non-core EDC features.
- Prepare EDC specifications, test plans, study-specific training materials, and other study-level documentation.
- Perform post-live EDC and reporting-application changes under change control.
- Apply CDASH and study protocols when creating EDC systems.
Requirements
- Zelta v2.0 experience is essential.
- Prior experience creating EDC systems and programming edit checks is required.
- Graduate or bachelor’s degree in life sciences, pharma, or a related health discipline from an accredited institution.
- Proficiency in CDASH and SDTM and their application to EDC system creation.
- CDASH certification is preferred.
- Effective communication, cooperation, teamwork, self-motivation, and the ability to work independently.
Benefits
- Full-time six-month contract.
- Position available at any of the company’s European locations.
- Collaborative work with clinical research, pharmacovigilance, and quality consulting teams.
