Description

Who We Are

BioMarin is a leading rare disease biotechnology company focused on genetically defined conditions.

Guided by our purpose to develop medicines that make a profound impact on people’s lives, our global teams have delivered a portfolio of therapies since our founding in 1997. Our revolutionary treatments for conditions like achondroplasia (the most common form of dwarfism), PKU (phenylketonuria), CLN2, a form of Batten disease, and a number of forms of MPS (mucopolysaccharidosis) offer new possibilities for patients and families who previously had few, if any, available options. More recently, with the close of the Amicus acquisition, our portfolio has expanded to include therapies for Fabry disease and Pompe disease, expanding our ability to reach more people living with rare genetic conditions.

Our success comes from our unwavering commitment to excellence, our deep understanding of patient needs, our scientific expertise, and our world-class manufacturing capabilities. At the heart of BioMarin is a dedicated team of the brightest minds in the industry working together to deliver innovative therapies to patients and families around the world.

About Worldwide Research and Development

From research and discovery to post-market clinical development, our R&D engine 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.

• Execute PKU medical MSL plans and tactics within assigned territory to meet scientific objectives and company-defined goals for products both marketed and in development
• Provide education relative to disease state, and BioMarin products across the PKU product lifecycle to health care providers, including dietitians, genetic counselors, nurses, researchers and other healthcare team members
• Serve as a medical/scientific resource through answering unsolicited medical questions and addressing other related medical information issues

• Engage in scientific exchange and provide feedback on emerging clinical/competitive trends 
• Identify, document, discuss and communicate insights to internal stakeholders  

• Maintain clinical and technical expertise in relevant therapeutic area

• Partner with medical and research and compliantly collaborate with commercial  

• Provide support to BioMarin clinical trials including but not limited to the following: site evaluation and identification; recruitment; investigator meetings; external expert identification; and study management
• Support the clinical department by communicating potential investigators for other BioMarin products in development
• Support the implementation and coordination of external investigator-initiated research 

• Participate in local, regional, and national meetings/conferences in support of all scientific and medical objectives
• Assist in the site level management of the publication plan timelines
• Work with internal Medical Affairs partners to develop and execute a territory plan designed to support and meet strategic medical objectives
• Input to and maintain internal documentation

• Review scientific journals, lead and participate in internal journal clubs 

• Serve as a scientific resource to commercial and marketing partners. Participate in sales team training, medical updates, scientific presentations, journal clubs, and other approved meetings
• Have responsibility for assigned special projects and mentoring of other team members 
• Self-development: Develops and communicates a professional growth plan. Takes responsibility for and actively manages professional development. Continually educates self on global market issues, trends, and product knowledge as it pertains to specific business responsibilities in key therapeutic areas
• Assure compliance with BioMarin operational guidelines

• 5 or more years of relevant clinical/industry experience 
• 3 or more years as an MSL is preferred  
• Experience in rare genetic diseases/PKU preferred
• Experience in product launch, development, and execution preferred
• Knowledge of regulations impacting Medical Affairs and field activities in the pharmaceutical industry
• Excellent oral and written communication, organization, and interpersonal skills 
• Proven track record as a team player   
• Project management/leadership experience 
• Ability to work in a virtual environment  
• Position may require up to ~60% travel for field and home office obligations but will be variable based on territory needs. Residency close to major transportation essential; California residency preferred. 

• Master's degree in a science required and terminal degree (doctoral level) preferred

Note: This description is not intended to be all-inclusive, or a limitation of the duties of the position. It is intended to describe the general nature of the job that may include other duties as assumed or assigned.

Equal Opportunity Employer/Veterans/Disabled

An Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability.