PK Scientist

3 weeks ago

London, Greater London, United Kingdom Pharmiweb Full time
Job Description

This is a exciting opportunity for a PK Scientist to join our team at ICON. We are looking for a highly motivated and experienced professional to lead the development of clinical pharmacology protocols and analysis plans.

Key Responsibilities:
  • Author and coordinate the development of clinical pharmacology protocols and analysis plans.
  • Provide quality control review of protocols and analysis plans.
  • Review dataset requirements for clinical studies with non-compartmental analysis.
  • Write the Clinical Pharmacology Analysis Plan (CPAP) based on the protocol.
  • Generate a logbook with data handling rules prior to the final NCA.
  • Perform preliminary, interim, and final PK, PD and/or PK/PD analysis for trials in all phases of drug development.
  • Create tables, listings and figures based on the CPAP.
  • Draft the clinical pharmacology sections of the Clinical Study Report.
  • Quality control of analysis, all delivered outputs, and documents reporting the analysis.

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