Principal Scientist, Pharmacometrics Support

Johnson & Johnson Innovative Medicine

Beerse, Belgium
Hybrid
R programming language expertise
Nonmem analysis input dataset generation
E-submission package preparation
Johnson & Johnson is seeking a Principal Scientist in Pharmacometrics Support to join their Innovative Medicine team in Beerse, Belgium. The role focuses on supporting Pharmacokinetic/Pharmacodynamic modeling and simulation activities in drug development, requiring expertise in R programming and a strong understanding of clinical drug development processes

Job Summary

  • This position is responsible to support the Pharmacometrics Leader (PML) or Clinical Pharmacology Leader (CPL) in the development and execution of Pharmacokinetic/Pharmacodynamic (PK/PD) Modeling and Simulation activities.
  • You will be responsible for preparing R programming scripts, generating analysis datasets, performing QC activities, and preparing e-submission packages for modeling analyses.
  • Interacting with other departments and external vendors to communicate data needs and promote better understanding across different departments is a key aspect of this role.

Matching Summary

Match Score: 85

Johnson & Johnson is seeking a Principal Scientist in Pharmacometrics Support to join their Innovative Medicine team in Beerse, Belgium. The role focuses on supporting Pharmacokinetic/Pharmacodynamic modeling and simulation activities in drug development, requiring expertise in R programming and a strong understanding of clinical drug development processes.

Skills & Requirements

Must-have

  • R programming language expertise
  • NONMEM analysis input dataset generation
  • e-submission package preparation
  • clinical drug development understanding
  • PK/PD population PK modeling concepts

Nice-to-have

  • AI driven approaches within data programming
  • cross-functional team environment
  • collaborate in a diverse global environment
  • AI assisted code generation working groups

Key Requirements

  • Master's degree with 6+ years experience or PhD with 4+ years experience
  • Good understanding of regulatory requirements and eCTD
  • Data-handling skills and solid understanding of SDTM and ADAM
  • Excellent written and oral communication skills
  • Ability to build and improve working relationships

Work Rights

Not specified

Tailored Resume

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