- Lead clinical pharmacology studies from phase 1 through to phase 3
- Facilitate translation from preclinical to clinical
- Preparing and reviewing clinical pharmacology sections of regulatory submission documents such as IB, IND, Briefing Books, NDA, etc.
- Ensure desired timelines and regulatory requirements
- Attend regulatory meetings and represent clinical pharmacology in regulatory interactions with Health Authorities


- PhD or equivalent experience in clinical pharmacology, pharmacokinetics or pharmacometrics
- At least 8 years of experience in clinical pharmacology
- Experienced with translational PK, PBPK and PK/PD
- Teamplayer and Multitasker