Cheiron
This role involves managing the regulatory lifecycle of approved products, working alongside AI to handle routine maintenance, complex case evaluations, and cross-functional projects. The position requires a global regulatory affairs expert to ensure regulatory accuracy throughout the product's lifecycle, from initial submissions to post-approval changes and documentation. The role focuses on supporting customers, defining platform requirements, and resolving edge cases in collaboration with the Life Sciences team.
Cheiron is a domain-tuned AI engine for biomedical and pharmaceutical professionals, delivering fast, verifiable, and context-aware insights across research, clinical, medical affairs, and regulatory workflows.
Headquarters
San Francisco, CA
Company Size
201-500 employees
Founded
2018
Industry
Technology
Glassdoor Rating
4.2 / 5
Sarah Johnson
Chief Executive Officer
Michael Chen
Chief Technology Officer
Emily Williams
VP of Engineering
David Rodriguez
VP of Product
Jessica Thompson
Chief Financial Officer
Andrew Park
VP of Sales
View leadership team, funding history,
and employee contacts for Cheiron.
Cheiron didn’t post a salary, so this is our estimate from similar listings.
23% below the average for this role
Global Regulatory Affairs Manager, 1-year contract
Ferring
Regulatory Affairs Manager
Integrated Resources INC
Regulatory Affairs (Pharma) Expert
lifelancer
Global Regulatory Affairs (CMC) Manager
Integrated Resources INC
Regulatory Affairs Associate (CMC Lifecycle)
Teva Pharmaceutical
Director, Regulatory CMC
Genetix Biotherapeutics