APAC Regulatory Submissions Lead

Fortrea is seeking a Regulatory Affairs professional in Auckland, New Zealand, to ensure compliance and oversight for clinical trial submissions. In this role, you will collaborate with stakeholders and provide critical guidance on regulatory issues and strategies.

The ideal candidate should possess at least 4 years of experience in the Pharmaceutical/CRO industry, specifically in Regulatory Affairs, with a Bachelor’s Degree in Life Sciences. The position offers hybrid work flexibility and involves some travel.