Pk Scientist

ICON Clinical Research, LP

Protocol development
Pharmacokinetic/pharmacodynamic (pk/pd) analysis
Non-compartmental analysis (nca)
Author and coordinate development of clinical pharmacology trial protocols and ensure timely review, approval, and issuance

Job Summary

  • Author and coordinate development of clinical pharmacology trial protocols and ensure timely review, approval, and issuance.
  • Perform preliminary, interim, and final PK, PD, and PK/PD analyses using non-compartmental methods.
  • Conduct QC review of protocols, analyses, datasets, and all deliverables while ensuring compliance with SOPs, ICH-GCP, and regulatory requirements.

Matching Summary

Author and coordinate development of clinical pharmacology trial protocols and ensure timely review, approval, and issuance.

Skills & Requirements

Must-have

  • protocol development
  • pharmacokinetic/pharmacodynamic (PK/PD) analysis
  • non-compartmental analysis (NCA)
  • clinical pharmacology reporting
  • Phoenix WinNonlin
  • ICH-GCP compliance

Nice-to-have

  • foster an inclusive environment
  • driving innovation and excellence
  • collaborating with cross-functional teams

Key Requirements

  • Bachelor's degree or higher in a scientific discipline
  • 1+ years of relevant experience
  • Working knowledge of data analyses software packages
  • working knowledge of R for PK/PD analysis
  • Basic knowledge of noncompartmental PK analysis

Work Rights

Not specified

Tailored Resume

Cover Letter