
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.
🔥 10 minutes ago
🗣️🇫🇷 French Required
🗣️🇳🇱 Dutch Required
Improve your chances of getting an interview by checking your resume score before you apply.

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 visits • 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 • Cover clinical research activities in Belgium, the Netherlands and potentially France
• College/University degree in Life Sciences or an equivalent combination of education, training & experience • Fluency in French, Flemish and English • Extensive on-site monitoring experience in phase 2/3 trials • Ideally, experience with complex trials in oncology or rare disease • Ability to plan, multitask and work in a dynamic team environment • Communication, collaboration, and problem-solving skills • Ability to travel
• Work-life balance • Collaborative, international team environment • Career growth opportunities • Trusted to take ownership early • Supportive team culture • Opportunity to help bring safe and effective pharmaceutical treatment to patients around the world
Apply Now