Life Science Internship Opportunity at BioMarin
Begin your biotech career with BioMarin as an Intern in Regulatory Information Management and Technology. This remote role offers hands-on exposure to global regulatory processes, data systems, and real-world tools used across the pharmaceutical and biotech industry. This Regulatory Affairs Role at BioMarin Careers is ideal for students seeking meaningful learning experiences in regulatory systems, data management, and innovative biotechnology environments.
Job Details:
- Position: Intern, Regulatory Information Management & Technology
- Location: United States, Remote
- Workstyle: Remote Only
- Department: Global Regulatory Affairs (GRA) โ RIMT Team
- Schedule: 40 hours/week
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Eligibility:
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Pursuing Bachelorโs degree in computerized systems, life sciences, or related fields
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Must return to school in Fall OR have graduated within 1 year
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Must be authorized to work in the U.S. without visa sponsorship
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About the Company:
BioMarin is a global biotechnology leader dedicated to transforming genetic discoveries into breakthrough medicines. Since 1997, the company has applied expertise in genetics and molecular biology to develop first-in-class and best-in-class therapies for patients with unmet medical needs. With a strong pipeline of commercial, clinical, and preclinical candidates, BioMarin fosters an empowering environment that encourages bold science and innovative thinking.
The Worldwide Research and Development (WWRD) engine drives all research effortsโfrom early discovery to post-market developmentโadvancing therapies for genetic diseases.
Educational Requirements for the Life Science Internship:
- Currently pursuing a Bachelorโs degree in Life sciences or a related field
- Must meet internship eligibility requirements (returning to school or graduated within 1 year)
Key Responsibilities of the Regulatory Affairs Role:
- Provide Regulatory Data Management and support the Regulatory Systems used by the Global Regulatory Affairs RIMT group
- Assist with Business Analysis to enhance data quality across Regulatory Information Management systems
- Assess and reconcile regulatory details for global Health Authority applications
- Support Operational Change Management related to technology improvements on the Veeva RIM platform
- Assist with document management, regulatory submissions, archival processes, and global registration records
Skills Required for the Life Science Internship:
Required Skills:
- Knowledge of Regulatory Affairs submission processes
- Proficiency in Microsoft Word, Excel, PowerPoint, Outlook
- Excellent written, verbal, and interpersonal communication skills
- Strong organizational and multitasking abilities
- Ability to work independently and collaboratively
Desired Skills:
- Familiarity with cloud data management systems
- Ability to analyze and synthesize data from multiple sources
- Understanding of data visualization and reporting concepts
How to Apply for the Regulatory Affairs Role?
Applications are accepted through the official BioMarin website. Candidates can submit their resume, verify eligibility, and stay updated on alerts for additional internship opportunities.
