Director, Global Medical Lead – Lysosomal Storage Disorders

October 4

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BioMarin Pharmaceutical Inc.

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Biotechnology • Pharmaceuticals

BioMarin Pharmaceutical Inc. is a leading global biotechnology company dedicated to transforming genetic discoveries into innovative medicines. Founded in 1997, the company has developed eight marketed products that address life-threatening genetic and lysosomal storage disorders such as achondroplasia and severe hemophilia A. BioMarin is also heavily invested in research and development, with a robust pipeline of investigational medicines at various clinical trial stages. The company's mission revolves around improving patient care by leveraging scientific expertise to understand the underlying causes of these conditions. BioMarin is committed to inclusivity and patient advocacy, engaging closely with communities to enhance care and quality of life for those with rare conditions.

1001 - 5000 employees

Founded 1997

🧬 Biotechnology

💊 Pharmaceuticals

💰 Post-IPO Debt on 2020-05

📋 Description

• The Global Medical Lead, Director level, is a critical leadership role in Global Medical Affairs, working on global activities for BioMarin's Enzyme Conditions portfolio. • Co-develops the Integrated Brand Plan (IBP) in partnership with the Commercial organization. • Offers scientific and medical expertise to inform the overall product strategy, contributing to clinical development, commercialization, and market access plans. • Leads development, execution, and communication of the Global Medical Plan in collaboration with other internal stakeholders across BioMarin. • Provides subject matter expertise as well as strategic leadership in key internal medical and clinical teams. • Ensures that all critical components of medical plans are executed and monitored for the intended impact. • Acts as product and disease area expert and primary contact point for global compound or disease area related issues.

🎯 Requirements

• MD, PhD, PharmD or other advanced life sciences degree required. • Extensive industry experience, especially in Medical Affairs (≥ 7 years) and Clinical Development, ideally in global role with experience in Genetic Medicine or LSDs/Rare Disease inherited metabolic conditions. • Ability to work, influence, and gain consensus across regions and cross-functional teams. • Demonstrate solid understanding of cross-functional inter-dependencies across the drug development lifecycle. • Excellent communication skills and a strong enterprise mindset required for problem solving and high-level presentations for senior executive staff review. • US and international experience working in orphan or specialty markets. • Knowledge and hands-on skills required to develop the strategy, framework, and scientific content for a wide range of post marketing studies. • Knowledgeable and current in GCP guidelines and compliance rules globally. • Clinical trial and publication experience is desirable. • Track record of successfully influencing without authority, partnering across functions especially with but not limited to Commercial. • Ability to understand the organization's financial goals, market landscape, and strategic objectives, and to apply that understanding to support scientific and strategic initiatives that deliver value to both patients and the company. • Able to thrive in an ambiguous and demanding environment, with high capacity for effective relationship building and teamwork. • Flexibility and adaptability. • Sensitivity to a multicultural environment. • Willingness to travel, mostly internationally. • English proficiency required.

🏖️ Benefits

• Equal Opportunity Employer/Veterans/Disabled