6 hours ago
Remote, EMEA or Prague, CzechiaMid 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.
- Create EDC specifications, test plans, study-specific training materials, and other study-level documentation.
- Perform post-live changes to EDC systems and related reporting applications under change control.
Requirements
- Essential experience with Medidata RAVE and Zelta v1.0.
- Prior experience creating EDC systems and programming edit checks.
- Graduate or bachelor’s degree in Life Sciences, Pharma, or a related health discipline from an accredited institution.
- Proficiency in CDASH and SDTM data standards and their application to EDC system creation.
- CDASH certification is preferred.
- Effective communication, cooperation, teamwork, self-motivation, and the ability to work independently.
Benefits
- The position is available in any of Ergomed’s European locations.
- Work in a collaborative clinical research organization focused on pharmaceutical development and patient outcomes.
Categories
About Ergomed
Ergomed is a contract research and pharmacovigilance services provider for pharmaceutical, biotechnology, and medical device companies. It delivers outsourced clinical development, data management (including EDC build), safety monitoring, and regulatory compliance, notably through its PrimeVigilance business. The company is privately held, operates globally, and is headquartered in Guildford, Surrey.