
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.
🔥 17 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.
• Plan, prepare, conduct, report, and follow up on Pharmacovigilance audits, including CAPA plans • Execute audits based on regulatory requirements and Good Pharmacovigilance Practice (GVP) • Perform GVP quality assurance projects for pharmaceutical and biotechnology client companies • Cover audits across Europe • Collaborate with a team of experts in clinical research, pharmacovigilance, and quality consulting
• Experience in conducting and leading internal and external Pharmacovigilance audits for a variety of stakeholders • Expert knowledge of national and international Pharmacovigilance legislation and guidelines • Proficient in managing projects and ensuring deliverables are provided timeously • Ability to identify issues and offer solutions in a pragmatic way • Bachelor’s Degree in Life Sciences preferred • Up to 40% travel • Ability to conduct remote audits
• Freelance position with full-time (1 FTE) or part-time (0.6 FTE and above) arrangements • Remote work options • Professional growth encouraged • Supportive, collaborative environment • Opportunity to make a real impact across the pharmaceutical and biotechnology industry • Work alongside respected life sciences companies • Up to 40% travel
Apply Now🕒 June 17
Associate Director - Auditor conducting audits for compliance in Computer System Validation, AI Assurance, and Data Integrity at ProPharma. Focused on regulatory sciences and client consulting across EMEA.