Senior Director, Clinical Regulatory Affairs

Description : Location :

This is an exempt full-time position and located in one of the following locations :

• Baar, Switzerland
• Chesterbrook PA, United States
• Portsmouth NH, United States

Candidates must be either currently located in the area or willing to relocate.

Position Summary :

We are seeking an experienced and strategic Sr. Director of Clinical Regulatory Affairs to lead and execute global clinical regulatory strategies for our Class III medical device programs. This leadership role will be critical in supporting clinical trial design, regulatory submissions, and interactions with global health authorities (e.g., FDA, EMA, PMDA) to enable successful development and approval of cutting-edge, high-risk medical devices.

Key Responsibilities :

Qualifications :

Preferred Experience

Leadership Competencies