- Bachelor’s degree in Pharma / Medical or another associated scientific discipline OR equivalent.
- Min. 4 years of experience in the Regulatory field and 2 years of demonstrated project management skills.
- Experience working with Microsoft Project or an equivalent program (preferred).
- Experience in driving/supporting submissions for major markets – US, EU, etc. (e.g., IND, NDA, BLA, EU MAA, EU variations, etc.) would be preferred.
Seniority Level
Associate
Employment Type
Full‑time
Job Function
Consulting
Industries
Pharmaceutical Manufacturing and Biotechnology Research