Contraline

The VP of Regulatory Affairs will develop and execute global regulatory strategies for innovative therapeutics and devices while serving as the primary contact for the FDA and other health authorities. This leader will build the regulatory function from the ground up and provide strategic input for corporate planning and investor communications.

The role serves as the single accountable owner for pharmaceutical Chemistry, Manufacturing & Controls (CMC) from Phase 3 through commercial launch. Responsibilities include defining manufacturing strategy, managing external partners, and ensuring regulatory CMC compliance for marketing applications.