Description
I have a requirement for a Regulatory Affairs Manager with a scientific background and extensive global project management experience for a major Pharma. The regulatory Affairs Manager role is on a 6 month contract for a MAJOR Pharma based in North Carolina.Key Factors:
-Extensive Regulatory Affairs Project Management
-Scientific Background - Scientific Degree ESSENTIAL
-Managing Cross Functional Teams
-FDA/NDA submission experience
-Ectd structure experience
-Project Management Exp
-3-5 years Reg Affairs Management exp
-Global Pharma exp
We need someone who can hit the ground running. My client can offer remote working once you have proven yourself. If you are interested, please attach an up to date CV and I will be in touch.