About the role
As an Associate Director you will lead the development and execution of global CMC regulatory strategies for the hematology and oncology portfolios. You will guide regulatory activities across development stages, mentor CMC Regulatory Affairs (RA) staff, supporting cross...
What you'll do
✓Own associate director, cmc regulatory affairs (hematology/oncology) work end-to-end, from first task to delivery
✓Collaborate daily with cross-functional teammates
✓Raise the bar on quality, performance and best practices
✓Share what you learn and help the team grow
What we're looking for
✓Mid-level experience in a similar Software engineer role
✓A track record of relevant, real-world work
✓Clear communication in a collaborative team
✓Ownership, curiosity and a sharp eye for detail
What we offer
Competitive salary, reviewed regularly
Flexible, hybrid-friendly schedule
Annual learning & development budget
Health insurance and wellness perks
Generous paid time off