Overview

A global biopharma company is seeking a skilled scientist to support non-clinical pharmacokinetics/pharmacodynamics (PKPD) and toxicokinetics strategy within early drug development. This role involves designing studies, analyzing data, and contributing to regulatory submissions.

Key Responsibilities

• Lead non-clinical PKPD and GLP toxicokinetics strategy and study design.
• Collaborate with cross-functional teams and CROs to ensure data quality.
• Analyze and report PKPD results using Phoenix WinNonlin and other tools.
• Deliver regulatory-standard reports and contribute to submission documents.

Ideal Candidate

• Degree in pharmacology, DMPK, or related field.
• 5+ years of hands-on PKPD experience in pharma or CRO.
• Proficient in Phoenix WinNonlin; R or Berkeley Madonna a plus.
• Strong communication and project management skills.

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