Director, Regulatory Affairs at Allucent

Allucent is hiring a Director, Regulatory Affairs to guide clients through drug, biologic, and medical device development; lead and mentor regulatory teams; shape regulatory strategies; manage complex regulatory projects; prepare Health Authority meeting requests and briefing documents; and author regulatory and scientific submissions. The role requires a scientific degree and at least eight years of regulatory experience involving US FDA, Health Canada, and/or European authorities, with advanced knowledge of CTD submissions and pre- and post-marketing regulatory requirements. The position offers remote or hybrid working depending on location, along with benefits, training, and career development opportunities.