Senior Scientist I, Clinical Pharmacology Sciences
Current- Key scientific contact for sponsors
- Review protocols and study designs
- Perform PK/PD analyses and write clinical study reports (Phase I – IIa Proof of Concept; e.g., Bioequivalence, First-in-Man, Thorough QT, Special Populations)
- Assess the impact of clinical/analytical events on study objectives from a PK/PD perspective
- Review reports generated by other Scientists
- Publish abstracts/manuscripts and present at scientific conferences