Candel Therapeutics
Remote Jobs
Candel is a clinical-stage biopharma company developing off-the-shelf, multimodal immunotherapies that stimulate personalized, systemic anti-tumor responses. Our platforms use genetically modified adenovirus and HSV constructs. With positive Phase 3 results for our lead candidate, it’s an exciting time to join us and help bring transformative cancer treatments to patients. Learn more: www.candeltx.com
3 Jobs
Associate Director, Regulatory Affairs
Candel TherapeuticsCandel is a clinical-stage biopharma company developing off-the-shelf, multimodal immunotherapies that stimulate personalized, systemic anti-tumor responses. Our platforms use genetically modified adenovirus and HSV constructs. With positive Phase 3 results for our lead candidate, it’s an exciting time to join us and help bring transformative cancer treatments to patients. Learn more: www.candeltx.com
The Associate Director, Regulatory Affairs will develop, communicate, and execute global regulatory strategies for assigned programs, leading the preparation of global regulatory submission plans across major markets like the US, EU, and Japan. This role involves serving as the primary regulatory point of contact for ex-US health authority interactions and overseeing the preparation and submission of CTAs and ex-US Marketing Applications.
Associate Director/Director, Regulatory Affairs CMC
Candel TherapeuticsCandel is a clinical-stage biopharma company developing off-the-shelf, multimodal immunotherapies that stimulate personalized, systemic anti-tumor responses. Our platforms use genetically modified adenovirus and HSV constructs. With positive Phase 3 results for our lead candidate, it’s an exciting time to join us and help bring transformative cancer treatments to patients. Learn more: www.candeltx.com
Serve as the CMC regulatory lead for viral vector-based gene therapy programs, developing and executing global regulatory strategies, authoring submission sections, and liaising with health authorities on manufacturing and quality matters. Collaborate with cross-functional teams and external partners to ensure regulatory alignment and support product lifecycle management.
The Associate Director, Regulatory Affairs
Candel TherapeuticsCandel is a clinical-stage biopharma company developing off-the-shelf, multimodal immunotherapies that stimulate personalized, systemic anti-tumor responses. Our platforms use genetically modified adenovirus and HSV constructs. With positive Phase 3 results for our lead candidate, it’s an exciting time to join us and help bring transformative cancer treatments to patients. Learn more: www.candeltx.com
Develop and execute global regulatory strategies for assigned development programs, spanning clinical development through marketing authorization and post-approval maintenance. This includes leading global submission plans, providing regulatory input to clinical development, and advising on regulatory implications of evolving data for major markets like the US, EU, UK, and Japan.
