
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.
🔥 1 hour ago
🗣️🇪🇸 Spanish Required
🗣️🇧🇷🇵🇹 Portuguese Required
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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.
• Perform on-site or remote Pre-Study, Initiation, Interim, and Close-Out monitoring visit activities in Spain and Portugal • Ensure facilities and investigational site staff remain adequate for study conduct • Identify investigators and verify their qualifications, resources, facilities, equipment, and staff throughout the study period • Train investigational site staff as necessary • Support preparation of regulatory and/or EC submissions when applicable
• College/University degree in Life Sciences or an equivalent combination of education, training & experience • Extensive on-site monitoring experience in phase 2/3 trials • Ideally, experience with complex trials such as oncology / rare disease • Full working proficiency in English, Spanish & Portuguese • Ability to plan, multitask and work in a dynamic team environment • Communication, collaboration, and problem-solving skills • Ability to travel
• Collaborative, international team environment • Career growth opportunities • Flexible working • Work-life balance • Opportunity to make an impact in meaningful clinical research • Supportive culture • Team of experts in clinical research, pharmacovigilance, and quality consulting
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