Regulatory Specialist – Regulatory Dossier Management

Are you an experienced Regulatory professional who enjoys driving complex global submissions and collaborating across functions? Join Regulatory Dossier Management and play a key role in bringing innovative treatments to people living with brain disorders - from early development through life-cycle management.

Your new role

You will be responsible for coordinating and leading the execution of global regulatory strategies for complex development projects. Working closely with global and local regulatory colleagues, you will represent Regulatory Dossier Management within cross-functional regulatory teams and help deliver Lundbeck's business objectives.

In this role, you will prepare and contribute to Clinical Trial Applications worldwide and coordinate the submission of initial Marketing Authorization...