Senior PKPD Programming Lead & Regulatory Submissions

A global biopharmaceutical company seeks an Associate Director to lead PKPD programming, ensuring high-quality deliverables and team management. The role requires a strong background in pharmacokinetics and pharmacodynamics, with over 10 years of experience in programming and regulatory submissions. Candidates should have expertise in using R and SAS, solid project management skills, and excellent communication abilities. This position offers a unique opportunity to influence drug development processes and mentor a skilled team. #J-18808-Ljbffr