Country Approval Specialist - Client dedicated

Become part of our team as a Country Approval Specialist, supporting the preparation and coordination of local regulatory submissions for clinical trials. You will guide local teams in aligning submissions with global strategies and provide regulatory advice. Ideal for candidates with relevant experience and strong communication skills.

Skills

• regulatory submissions
• french language
• regulatory strategy
• ethics committee submissions
• patient information sheet development
• informed consent form development
• regulatory compliance review
• clinical trial coordination
• project coordination
• english language
• medical terminology
• regulatory guidelines knowledge
• sop compliance
• database entry
• feasibility coordination
• negotiation
• teamwork
• planning
• computer skills