Principal Scientist, Pharmacokinetics (pk)

Century Center

**
Phd in pharmaceutical sciences or related field
5+ years pharmaceutical development experience
Expertise in pk/pd modeling and simulation
** The Principal Scientist, Pharmacokinetics position at Century Center involves leading nonclinical PK/QSP strategies for drug development projects, providing scientific leadership, and collaborating with interdisciplinary teams. The ideal candidate should have a PhD in Pharmaceutical Sciences, significant pharmaceutical development experience, and proficiency in modeling and simulation applications. **

Job Summary

  • The Principal Scientist PK/QSP will lead nonclinical pharmacokinetics and quantitative systems pharmacology strategies across multiple drug development projects.
  • This role requires designing study protocols, performing advanced mechanistic modeling, and providing scientific leadership from early discovery through market authorization.
  • CSL Behring is a global biotherapeutics leader committed to saving lives through innovative therapies in immunology, hematology, and other critical areas.

Matching Summary

Match Score: 75

** The Principal Scientist, Pharmacokinetics position at Century Center involves leading nonclinical PK/QSP strategies for drug development projects, providing scientific leadership, and collaborating with interdisciplinary teams. The ideal candidate should have a PhD in Pharmaceutical Sciences, significant pharmaceutical development experience, and proficiency in modeling and simulation applications. **

Skills & Requirements

Must-have

  • PhD in Pharmaceutical Sciences or related field
  • 5+ years pharmaceutical development experience
  • Expertise in PK/PD modeling and simulation
  • Proficiency with Phoenix WinNonLin NONMEM R
  • Knowledge of GLP regulations and ICH guidelines

Nice-to-have

  • Experience across multiple therapeutic areas
  • Familiarity with CSL disease therapeutic areas
  • Experience working in multicultural international teams
  • Track record in regulatory submissions

Key Requirements

  • Minimum 5+ years of pharma/biotech/CRO experience
  • Training in industry standard software packages
  • Proven track record in nonclinical assessments

Work Rights

Not specified

Tailored Resume

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