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Full-Time

Senior Director

Clinical Regulatory Affairs

Confirmed live in the last 24 hours

Arcellx

Arcellx

51-200 employees

Develops cell therapies for cancer, autoimmune diseases

Hardware
Biotechnology

Compensation Overview

$280k - $310kAnnually

+ Bonus + Equity (RSU) Grant + Relocation Assistance + Medical Coverage + Dental Coverage + Vision Coverage + Unlimited Vacation + Parental Leave + Tuition Reimbursement + 401k Contribution

Expert

San Carlos, CA, USA

Category
Healthcare Administration & Support
Medical, Clinical & Veterinary
Required Skills
Communications
Requirements
  • BSc in natural or health sciences
  • 12-15+ years of clinical regulatory affairs experience
  • Proficiency in writing submission documents
  • Experience interacting with Health Authorities
  • Solid understanding of biology, chemistry, or engineering
  • Exceptional project management skills
  • Excellent written and verbal communication skills
Responsibilities
  • Develop and execute global clinical regulatory strategies
  • Lead program teams in preparing regulatory submissions
  • Oversee strategy and drafting of documents for regulatory authority interactions
  • Maintain knowledge of global regulatory environment
  • Support internal clinical and development teams with global regulations

Arcellx develops innovative cell therapies for cancer and autoimmune diseases, leveraging their novel D-Domain technology and transformative ddCAR and ARC-SparX platforms to enhance cell therapy.

Company Stage

N/A

Total Funding

$736M

Headquarters

Gaithersburg, Maryland

Founded

2014

Growth & Insights
Headcount

6 month growth

5%

1 year growth

13%

2 year growth

63%