The Global Regulatory & CMC Lead is responsible for the development and implementation of regulatory strategies for specific projects, while serving as the regulatory representative on the respective program teams. This includes Karyopharm’s key clinical programs, international submissions in collaboration with our multiple alliance partners, and all CMC initiatives and submissions.
Reporting to our Senior Vice President, Regulatory Affairs, you will positively impact patients’ lives with the following contributions:
If you want to do something that matters, this work matters. Patients drive our passion to pioneer novel cancer therapies. That’s why we’ve built an environment centered around support, flexibility, and a shared mission.
Creating and delivering medicine for cancer can only be done through focus, dedication, and heart. We hire exceptional people and trust each other to work in whatever way lets us, be us – whether that’s onsite, from home, or anywhere in between.
What do you get when you pair an extraordinary mission with a culture of flexibility and empowerment? We invite you to find out and join us on this incredible mission.
Check out our Culture Video!
What We Offer:
In addition to our exciting, supportive, and intellectually challenging global workspaces(s), teamembers enjoy a comprehensive and generous benefits package (active on day one) that makes them more productive and contributes directly to the development of their professional skills.
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