With accelerated review underway in the United States and Europe for our Hemophilia A drug, a second gene therapy program entering the clinic for PKU patients, and a third program in late research for Hereditary Angioedema, BioMarin continues to pioneer innovative approaches to treating rare diseases. Our commitment to gene therapy is further underscored by having developed the first and largest gene therapy manufacturing facility in the world. The scientific possibilities and the hope we offer to patients with rare diseases is enormous.
BioMarin is a midsize biotechnology company with a market cap of approximately 18 billion. Over the course of our 22 year history we have successfully launched 7 drugs for the treatment of rare diseases. Our success is due to our scientific rigor and our ability to leverage multiple therapeutic modalities. BioMarin is based in the San Francisco Bay Area and offers a comprehensive relocation program.Success Profile
Check out the traits we’re looking for and see if you have the right mix.
" BioMarin has this, in their own DNA, an approach: they only work on projects for which they know the underlying biology." Lon C., Chief Scientific Officer
"We’ve got to understand: What are the problems other people are trying to solve? And do we have a better way of fundamentally doing that?" Brinda B, GVP, Corporate and Business DevelopmentTrending Videos Responsibilities
BioMarin is the world leader in delivering therapeutics that provide meaningful advances to patients who live with serious and life-threatening rare genetic diseases. We target diseases that lack effective therapies and affect relatively small numbers of patients, many of whom are children. These conditions are often inherited, difficult to diagnose, progressively debilitating and have few, if any, treatment options. BioMarin will continue to focus on advancing therapies that are the first or best of their kind.
BioMarin’s Research & Development group is responsible for everything from research and discovery to post-market clinical development. Research & Development involves all bench and clinical research and the associated groups that support those endeavors. Our teams work on developing first-in-class and best-in-class therapeutics that provide meaningful advances to patients who live with rare diseases. Come join our team and make a meaningful impact on patients’ lives.
EU Regulatory Affairs team members works with US based project teams and subject matter experts to support the clinical development and life cycle management of gene therapy medicinal products. They are responsible for the timely generation of high quality submissions to support clinical trial initiation and market applications in the U.S., EU and multiple international. This role involves working closely with CMC teams, regulatory CMC individuals, and interactions with global health authorities to provide input and achieve alignment on the regulatory strategies for gene product development and commercialization. A level of expertise and knowledge of global regulations, guidance for the development of gene therapy products and strong technical expertise is desired.
Ph.D. in biological or physical science is preferred. MS/BS is acceptable with appropriate relevant experience.
From internationally renowned scientists to patient advocates, BioMarin Hemophilia has brought together the right people.
BioMarin has entered into a preclinical collaboration and license agreement with DiNAQOR, a gene therapy platform company, to develop novel gene therapies to treat rare genetic cardiomyopathies.
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