
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.
November 21

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.
• Provide Regulatory Data Management and Regulatory Systems Usage/Implementation assistance for Global Regulatory Affairs RIMT group. • Utilizing Information Management skills, provide Business Analysis to assist in enhancing existing Regulatory Information management data quality. • Envisioned projects include: Assess and reconcile regulatory details associated with Regulatory Health Authority Applications to support both Marketing and Investigational Drug Product authorizations. • Providing support for Operational Change Management activities relating to technology improvements related to the Veeva RIM platform.
• Knowledge of the Regulatory Affairs submission process • Proficient computer skills and working knowledge of Microsoft Office (Word, Excel, PowerPoint and Outlook) • Excellent interpersonal, written and verbal communication skills • Strong organizational skills with ability to prioritize and manage tasks in a fast-paced environment • Ability to work independently and collaboratively • Familiarity with cloud data management systems • Ability to analyze, transform, and synthesize data from multiple sources into a single system • Familiarity with Data Visualization and Reporting Concepts • Student pursuing a Bachelor’s degree in computerized systems or life sciences (or in related fields of study). • Student must be returning to school in the Fall Term OR has graduated within the 1 year of the start of the program. • Must be available to work 40 hours a week • Must be authorized to work in the United States without visa sponsorship.
• Paid hourly wage • Paid company holidays • Sick time • Opportunities for professional development by building relationships and learning about other parts of the business. • Participate in company all hands meetings, monthly community lunches • Assistance with housing/transportation to help alleviate costs associated with the internship for eligible employees.
Apply NowNovember 8
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