
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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🗣️🇫🇷 French Required
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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.
• Perform on-site or remote Pre-Study, Initiation, Interim, and Close-Out monitoring visits • Ensure investigational-site facilities and 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 • Travel nationally and to France and Belgium, including the French-speaking part of Belgium
• College/University degree in Life Sciences or equivalent combination of education, training and experience • Extensive on-site monitoring experience in Phase 2/3 trials • Ideally, experience with complex trials such as oncology or rare disease • Full working proficiency in English and French • Ability to plan, multitask, and work in a dynamic team environment • Communication, collaboration, and problem-solving skills • Ability to travel
• Remote work option • Collaborative, international team • Career growth opportunities • Work-life balance • Opportunity to help bring safe and effective pharmaceutical treatment to patients around the world • Passionate and collaborative team of experts • Inclusive workplace where everyone is welcome and every voice counts
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