
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.
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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.
• Plan, prepare, conduct, report, and follow up on various types of GCP audits according to expected quality and timelines • Execute audits based on comprehensive understanding of regulatory requirements and Good Clinical Practice (GCP) • Perform GCP quality assurance projects on behalf of pharmaceutical and biotechnology client companies • Conduct and lead internal and external GCP audits • Conduct service provider and GCP systems audits • Coordinate and manage inspection preparation activities for GCP process inspections at sponsor and investigator sites
• BSc in Life Science preferred • Experience in conducting and leading internal and external GCP audits for a variety of stakeholders • Experience conducting service provider audits, including full-service CRO, biostatistics, data management, and phase I audits • Experience conducting GCP systems audits • Experience coordinating and managing inspection preparation activities for GCP process inspections at sponsor and investigator sites • Expert knowledge of national and international GCP legislation and guidelines • Ability to travel up to 40% • Ability to conduct remote audits
• Up to 40% travel • Ability to conduct remote audits • Supportive, collaborative environment • Professional growth encouraged • Opportunity to make a real impact across the life sciences industry • Collaborative team of experts in clinical research, pharmacovigilance, and quality consulting
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