Associate Director/Director, Regulatory Affairs CMC
Candel TherapeuticsMassachusetts, United States
Posted March 10, 2026
160000 - 200000 USD
Full Time
About the Company
Candel is a clinical-stage biopharma company developing off-the-shelf, multimodal immunotherapies that stimulate personalized, systemic anti-tumor responses.
Job Description
We are a clinical-stage biopharma company developing off-the-shelf, multimodal immunotherapies that stimulate personalized, systemic anti-tumor responses. The Associate Director/Director, Regulatory Affairs CMC will serve as the CMC regulatory lead for one or more viral vector-based gene therapy programs.
Requirements
- Bachelor's degree in a scientific discipline (e.g., Biochemistry, Molecular Biology, Chemistry, Pharmacy, Chemical Engineering)
- 8+ years of progressive experience in regulatory affairs within the biopharmaceutical industry
- At least 3 years of direct experience with biologics (cell and/or gene therapy products and viral vector-based preferred)
- Excellent written and verbal communication skills
- Proven leadership and interpersonal skills
- Strategic thinker with strong problem-solving and decision-making abilities
Benefits
- Base salary: $160,000- $200,000
- Remote work option
- Eastern or Central U.S. core hours
- Benefits listed are not explicitly stated, but may include health insurance, retirement plan, paid time off, etc.
