Global Regulatory Affairs Lead, Associate Director
kailera therapeuticsWaltham (MA)
Global Regulatory Affairs Lead, Associate Director
Posted 2 days ago
kailera therapeuticsWaltham (MA)
SENIORITY
Manager
About the role
Kailera Therapeutics is seeking an Associate Director, Global Regulatory Affairs to lead day-to-day regulatory activities for early and late-stage investigational products, guiding IND/CTA submissions and future marketing applications. Have you got the right qualifications and skills for this job Find out below, and hit apply to be considered. You will partner with Regulatory CMC and Operations to align data with agency expectations. Required location: Waltham, MA, hub-based onsite 3-4 days/week. xmcpwfuA Bachelor's with 10+ years or an Advanced degree with 5+ years in drug development is required.
Before you apply
Applying takes about a minute. These four things decide how fast it moves after that.
Your profile is current
It's what we read first. Occupations, seniority and locations matter more than a long history.
Two examples you can talk through
Not a portfolio — just two pieces of work where you can explain the decisions and what you'd change.
A number in mind
What you're on now and what would make you move. We negotiate better when we know both.
Your notice period
Employers plan around it, and it's the question that stalls offers most often.
Once you apply, someone reads it and calls you before anything reaches the employer — usually within two working days.