Regulatory Affairs Director required by Barrington James for an initial 12-month, remote contract opportunity with the client based in South San Francisco. This contract will be about 30 hours a week. You must be based on the West Coast to be considered for this role. You will need to have strong experience in FDA interaction, NDA filings, rare disease and orphan drug experience within small molecule.If you have worked with Hepatology that would be advantageous. Additionally prior work with EU PIP would be beneficial.