Senior Regulatory Project Manager, Biotech

biomarin; San Rafael (CA); On-site; USD 130,000 - 165,000; Full time

Job summary

BioMarin is seeking a Regulatory Senior Project Manager to drive regulatory strategy and cross‑functional collaboration across global teams. This role sits in the Global Regulatory Affairs & Patient Safety (GRAPS) department and supports timelines from pre‑clinical through product life cycle.

The ideal candidate holds a health/life sciences degree (Masters/MBA preferred) with 6+ years of project management experience in biotech/pharma, and excels in communication and leadership within a

Qualifications

• Degree in health or life sciences; Masters or MBA preferred.
• 6+ years with Masters/MBA, 8+ with bachelor’s degree.
• Project Management experience in biotech or pharmaceutical environment preferred.

Responsibilities

• Strategy and Execution: contribute to regulatory strategy and timelines; manage action items; collaborate with GRL and regulatory leads.
• Meeting Management & Support: schedule GRT meetings, generate agendas, record minutes; support MA/IND/CTA filing teams.
• Cross-functional Leadership: liaise across regulatory teams and cross‑functional filing teams; represent Regulatory in PRIME and dashboards.

Skills

Regulatory leadership

Project management

Cross‑functional leadership

Strategic thinking

Communication

Team management

Education

Degree in health or life sciences (Masters or MBA preferred)

Job description

BioMarin is seeking a Regulatory Senior Project Manager to drive regulatory strategy and cross‑functional collaboration across global teams. This role sits in the Global Regulatory Affairs & Patient Safety (GRAPS) department and supports timelines from pre‑clinical through product life cycle.

The ideal candidate holds a health/life sciences degree (Masters/MBA preferred) with 6+ years of project management experience in biotech/pharma, and excels in communication and leadership within a