
Biotechnology • Pharmaceuticals • Healthcare Insurance
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.
October 21

Biotechnology • Pharmaceuticals • Healthcare Insurance
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.
• Responsible for leading and overseeing all operational aspects of global pharmacovigilance activities • Ensure compliance with regulatory requirements, company SOPs, and industry standards • Manage PV teams, optimize operational processes • Collaborate cross-functionally to ensure the highest level of patient safety and product quality • Define KPIs and monitor team performance • Champion a culture of excellence across global PV operations • Collaborate with various PMO teams to optimize and standardize end-to-end pharmacovigilance processes. • Drive global harmonization of PV processes across regions, affiliates, and partners to ensure consistent execution and regulatory alignment • Lead inspection readiness and quality excellence initiatives
• Ideally an Advanced degree • 15 + years of pharmacovigilance experience, with at least 10 years in an operational leadership role with P&L responsibilities. • In-depth knowledge of global PV regulations, GVP modules, and drug safety principles. • Proven track record of managing PV operations in a global environment within a CRO or PV service provider. • Strong leadership, project management, and strategic thinking skills. • Excellent communication, negotiation, and interpersonal abilities. • Experience with safety databases (e.g., Argus, ArisG) and PV software tools.
• Training and career development opportunities internally • Strong emphasis on personal and professional growth • Friendly, supportive working environment • Opportunity to work with colleagues based all over the world, with English as the company language
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