Associate Director, Global Regulatory Lead
CRISPR Therapeutics(2 months ago)
About this role
The Global Regulatory Lead (Associate Director/Director) at CRISPR Therapeutics will join the R&D organization to guide regulatory strategy for gene- and cell-therapy product candidates across global markets. The role focuses on shaping regulatory approaches to advance programs from early development through regulatory submissions and approvals while contributing to organizational growth in a fast-moving biotech environment.
Required Skills
- Regulatory Strategy
- Regulatory Submissions
- Regulatory Writing
- Agency Interactions
- Product Development
- Cross-Functional
- Data Analysis
- Communication
- Leadership
- Clinical Development
Qualifications
- Bachelor's Degree in Pharmacy, Biology, Chemistry or Pharmacology
- MS
- MBA
- PhD
- MD
Apply instantly with AI
Let ApplyBlast auto-apply to jobs like this for you. Save hours on applications and land your dream job faster.
More jobs at CRISPR Therapeutics
Similar Jobs
Director, Global Regulatory Affairs, Neuroscience
Takeda Pharmaceutical Company(1 month ago)
Scientist II/Senior Scientist Nonclinical Development
Epicrispr Biotechnologies(1 month ago)
Director, CMC Regulatory
Umoja Biopharma(1 month ago)
Regulatory Submissions Manager (EU CTR)- Turkiye
Clinical Careers Page(10 days ago)
Associate Director, Global Regulatory Lead, Oncology
Takeda Pharmaceutical Company(3 months ago)
Clinical Trial Regulatory Specialist
Clinical Careers Page(4 days ago)