
1001 - 5000 employees
Founded 1997
đź’Ľ 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
đź’Ľ 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.
• Provide administrative support for meetings and invoice activities • Generate reports • Maintain Medical Information systems and department documentation • Engage in pharmacovigilance and quality complaint follow-up activities • Provide administrative support for Medical Information Enquiries, Adverse Event, and Product Quality Complaint activities • Support new client onboarding activities • Assist with departmental regulatory inspection preparedness • Support the Medical Information team with various administrative duties
• Advanced English skills, both verbal and written, at least B2 • Desirable administrative experience • Good IT skills, including MS Office • High degree of discretion when dealing with confidential information • Ability to manage multiple and varied tasks and prioritize workload with attention to detail • Ability to work under pressure with accuracy and meet tight deadlines • Good interpersonal and communication skills
• Full-time employment • Remote work option • Collaborative and supportive work environment • Flexible work culture • Growth and development opportunities • Global team and international work environment • Opportunity to contribute to patient safety and pharmaceutical treatment • Passionate and collaborative team of experts in clinical research, pharmacovigilance, and quality consulting
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