EDC Developer – Medidata RAVE, Zelta v1.0

🔥 18 hours ago

🌐 New Zealand, United Kingdom – Remote

🇳🇿 New Zealand – Remote 🇬🇧 United Kingdom – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

🖥 Software Engineer

👻 Ghost score 17%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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ERGOMED

WebsiteLinkedInAll Job Openings

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.

📋 Description

• Create EDC systems including structure, workflow, edit checks, and user roles and permissions based on CDASH data standards, study protocols, and standard eCRF templates • Build additional EDC functionality where applicable, including randomisation, ePRO, IMP management, and targeted SDV • Manage ePRO licensing, validation, and translation where applicable • Create study-level EDC system 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

🎯 Requirements

• Medidata RAVE and Zelta v1.0 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 is required • Effective communication skills • Cooperative and team-oriented approach • Self-motivation and ability to work independently • Proficiency in data standards CDASH and SDTM and their application to EDC system creation • CDASH Certification preferred

🏖️ Benefits

• Remote work options • Opportunity to work with a passionate and collaborative team of experts in clinical research, pharmacovigilance, and quality consulting • Diverse and inclusive workplace where every voice counts • Career growth opportunities • Opportunity to make a difference to patients' lives