Country Approval Specialist - FSP

We are seeking a Country Approval Specialist to support the preparation and coordination of local regulatory submissions for oncology and cell therapy clinical trials. You will guide submissions in line with global strategies and provide local regulatory advice. Ideal for candidates with relevant experience and strong communication skills.

Skills

• regulatory submissions
• ethics committee submissions
• clinical trial site activation
• regulatory strategy
• patient information sheet development
• informed consent form development
• regulatory compliance review
• ppd sops
• client sops
• medical terminology
• oncology/cell therapy knowledge
• negotiation skills
• attention to detail
• planning skills
• computer skills
• english language proficiency