Full-Time

Senior Director

Clinical Regulatory Affairs

Updated on 4/26/2024

Arcellx

Arcellx

51-200 employees

Develops cell therapies for cancer, autoimmune diseases

Biotechnology

Compensation Overview

$280,000 - $310,000Annually

+ Annual Bonus + Equity (RSU) Grant + Relocation Assistance

Senior

San Carlos, CA, USA

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 interactions with regulatory authority
  • Maintain detailed 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

Redwood City, California

Founded

2014

Growth & Insights
Headcount

6 month growth

10%

1 year growth

28%

2 year growth

76%