EMEA Regulatory Submissions Manager: Strategic Compliance

Fortrea is seeking a Regulatory Affairs professional to lead RA, IRB/EC, and Third Body submissions across projects. You will manage submission strategies, timelines, and country packages while coordinating responses to inquiries and ensuring regulatory compliance.

Applicants should have 5+ years in pharma regulatory affairs, strong project management and supervisory experience, and a degree in Life Sciences. This role supports audits, risk management and ongoing regulatory guidance.