Opportunity Details

The Global Regulatory Affairs Vice President - Clinical position at the client involves developing and executing regulatory strategies for metabolic disease drug development, ensuring compliance with FDA, EMA, and global regulatory requirements. The role requires overseeing clinical regulatory affairs, driving interactions with regulatory agencies, and providing strategic guidance on regulatory pathways and trends affecting metabolic disease treatments. The successful candidate should have 10+ years of regulatory affairs experience in biopharma, with a focus on metabolic disease indications, a proven track record of successful FDA and EMA interactions, and expertise in late-stage development and approval processes.

The client is a large organization in the Life Sciences industry known for its innovative approach to quality and global presence. The company's major pipeline focus is on diabetes and obesity treatments. The Global Regulatory Affairs Vice President - Clinical will work cross-functionally with clinical, medical, and commercial teams to optimize regulatory positioning, manage regulatory submissions, and ensure timely approvals. The position offers a salary range of $350,000 - $440,000, a comprehensive benefits package, and extensive career growth opportunities. If you are an experienced clinical Regulatory Affairs expert in the Life Sciences industry looking to make a significant impact on a global scale, we encourage you to apply for this position.