BioMarin Pharmaceutical Inc.
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
Medical Director
Job not on LinkedIn
Yesterday
BioMarin Pharmaceutical Inc.
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
• Perform medical review of pre- and post-marketing individual case safety reports (ICSRs) • Collaborate with Clinical Science, Medical Affairs, PV colleagues and applicable functional specialists • Participate in the development of safety surveillance and risk management plans for drug development programs • Serve as medical safety expert and liaise with clinical study/project teams
🎯 Requirements
• Medical degree (e.g., MD, DO) with appropriate clinical and pharmacovigilance experience • Minimum 5 years’ experience in PV with specific drug safety operational experience • Excellent medical knowledge • Strong working knowledge of US and ex-US PV requirements • Experience with pre- and post-marketing ICSR processing and aggregate safety reporting
🏖️ Benefits
• Health insurance • 401(k) • Flexible work arrangements • Professional development opportunities
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