
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.
October 30

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.
• Drafts and edits documents used in conducting and reporting the results of clinical studies. • Manages study team participation in preparation of regulatory filings. • Builds effective partnerships with cross-functional groups to ensure customer/stakeholder needs are met. • Provides peer review and editing support for other regulatory documents.
• Bachelor’s or higher degree required; scientific focus desirable. • Up to 6 years of experience as a medical writer in the pharmaceutical industry. • At least 10 years of medical or scientific writing experience as a primary job responsibility. • Advanced understanding of the drug development process, biostatistical and clinical research concepts. • Experience writing, reviewing, or editing protocols and clinical study reports required. • Experience writing, reviewing, or editing INDs, BLA/NDAs, PBRERs, DSURs, and PAERs highly preferred.
• Equal Opportunity Employer/Veterans/Disabled
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