
1001 - 5000 employees
Founded 1997
💼 Consulting
🏥 Healthcare
📦 Logistics
Consulting • Healthcare • Logistics
ERGOMED is a global group providing specialized services to the biotechnology and pharmaceutical industries. It operates under different service lines, including Ergomed Clinical Research, PrimeVigilance, and ADAMAS Consulting, and is dedicated to providing full-service clinical research organization (CRO) capabilities. Focused on oncology, rare diseases, and complex trials, it also offers end-to-end pharmacovigilance and medical information services, as well as comprehensive GxP audits. Ergomed is committed to supporting drug development with a global presence in around 100 countries.
🔥 0 minutes ago
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1001 - 5000 employees
Founded 1997
💼 Consulting
🏥 Healthcare
📦 Logistics
Consulting • Healthcare • Logistics
ERGOMED is a global group providing specialized services to the biotechnology and pharmaceutical industries. It operates under different service lines, including Ergomed Clinical Research, PrimeVigilance, and ADAMAS Consulting, and is dedicated to providing full-service clinical research organization (CRO) capabilities. Focused on oncology, rare diseases, and complex trials, it also offers end-to-end pharmacovigilance and medical information services, as well as comprehensive GxP audits. Ergomed is committed to supporting drug development with a global presence in around 100 countries.
• Create EDC systems, including structure, workflows, edit checks, and user roles and permissions, based on CDASH data standards, study protocols, and standard eCRF templates • Build applicable additional EDC functionality, including randomisation, ePRO, IMP Management, and targeted SDV • Create study-level EDC documentation, including specifications, test plans, and study-specific training materials • Perform post-live changes to EDC systems and applicable reporting applications under the Change Control process • Work under the direction of the Director of Data Management with project-level oversight from the Project Data Manager
• Zelta v2.0 experience is essential • Graduate or bachelor’s degree in Life Sciences, Pharma, or a related health discipline from an accredited university or college • Prior experience in EDC system creation and Edit Check programming • Effective communication skills • Cooperative and team-oriented approach • Self-motivation and ability to work independently • Proficiency in data standards (CDASH & SDTM) and their application to EDC system creation • CDASH Certification preferred
• Remote work availability • Collaborative team environment • Opportunities for growth • Diverse and inclusive workplace • Work contributing to safer pharmaceutical treatments for patients
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