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.
#J-18808-LjbffrEMEA Regulatory Submissions Manager: Strategic Compliance employer: Fortrea
Fortrea is an exceptional employer that fosters a dynamic and collaborative work culture in Maidenhead, England. With a strong emphasis on employee growth and development, we offer comprehensive training programs and opportunities for advancement within the pharmaceutical sector. Our commitment to innovation and client success ensures that you will play a pivotal role in shaping the future of healthcare while enjoying a supportive environment that values your contributions.
