
Principal Scientist PKPD
- Reading
- Contract
- Full-time
- Develop and lead non-clinical PKPD and GLP toxicokinetics study strategies.
- Design and write protocols for regulatory studies, providing scientific input.
- Collaborate with project teams and CROs to ensure high-quality data generation.
- Work under GLP compliance to deliver regulatory-standard data packages.
- Communicate interim and final PKPD-toxicokinetic data analysis results to stakeholders.
- Deliver comprehensive PKPD study reports and contribute to submission documents.
- Build a thorough understanding of drug pharmacology and PKPD to facilitate candidate advancement.
- Represent the department internally and externally, enhancing its scientific reputation.
- Background in quantitative pharmacology, pharmacokinetics/pharmacodynamics, or DMPK (PhD/MSc/BSc).
- Hands-on experience in PKPD data analysis within a pharma or CRO environment.
- Strong understanding of pharmacology and drug mechanisms related to disease.
- Proven ability to design, execute, and analyze non-clinical PKPD studies, including GLP toxicokinetics.
- Proficiency in Phoenix WinNonlin for PKPD analysis; familiarity with tools like Berkeley Madonna or R is a plus.
- Excellent communication skills, with the ability to produce high-standard reports for regulatory submissions.
- Experience working in matrix environments and managing multiple projects simultaneously.
- A record of publications or external scientific contributions in PKPD is advantageous.
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