The company is dedicated to curing cancer through pioneering personalized CAR T-cell therapies
Job Summary
The company is dedicated to curing cancer through pioneering personalized CAR T-cell therapies.
This role involves driving cross-functional submission teams and managing regulatory deliverables for the global Regulatory CMC team.
Candidates will benefit from a comprehensive benefits package including medical, dental, vision, life insurance, and potential discretionary bonuses.
Matching Summary
The company is dedicated to curing cancer through pioneering personalized CAR T-cell therapies.
Salary
Base: $123,930.00 - $160,380.00; Bonus/Equity: Discretionary annual bonus and stock-based incentives eligible; Benefits: Medical, dental, vision, life insurance, and paid time off
Skills & Requirements
Must-have
5+ years project management experience
Regulatory submission timeline management
Cross-functional team coordination skills
MS Office and SharePoint proficiency
Nice-to-have
Module 3 regulatory experience preferred
Veeva Vault platform knowledge
AI tools experience
Cell therapy industry background
Key Requirements
BA/BS degree with 5+ years experience OR MA/MS/MBA with 3+ years
Knowledge of drug development process and Regulatory CMC practices
Proficiency in MS Word, Excel, PowerPoint, Outlook, Teams, and SharePoint