Dmpk Scientist

Arvinas

New Haven, CT, USA
Not specified; not specified; comprehensive benefi...
Remote
Ph.d. in pharmaceutical science or related field
10+ years dmpk experience in biopharma
In vitro and in vivo adme expertise
The role involves contributing to drug discovery through all stages of development, including early ADMET profiling and lead candidate selection

Job Summary

  • The role involves contributing to drug discovery through all stages of development, including early ADMET profiling and lead candidate selection.
  • Arvinas utilizes its proprietary PROTAC platform to engineer targeted protein degraders for treating debilitating diseases like cancer and neurodegenerative disorders.
  • Employees are expected to partner with CROs to develop customized ADMET assays and prepare DMPK components for regulatory documents such as IND submissions.

Matching Summary

The role involves contributing to drug discovery through all stages of development, including early ADMET profiling and lead candidate selection.

Salary

Not specified; Not specified; Comprehensive benefits program including medical, vision, dental

Skills & Requirements

Must-have

  • Ph.D. in pharmaceutical science or related field
  • 10+ years DMPK experience in biopharma
  • In vitro and in vivo ADME expertise
  • Animal PK and toxicokinetics knowledge
  • Drug-drug interaction assessment skills
  • PK analysis with Phoenix software

Nice-to-have

  • Experience with PROTAC or molecular glue
  • ADC drug development background
  • PBPK or PK/PD modeling proficiency
  • Regulatory document preparation experience
  • CRO partnership management skills

Key Requirements

  • Ph.D. required with 10+ years relevant experience
  • Must have ability to work without visa sponsorship
  • Proficiency in PK analysis software like Phoenix
  • Knowledge of GLP and regulatory guidance
  • Direct experience with PROTAC or ADC desirable

Work Rights

Must be eligible to work in the US without visa sponsorship

Tailored Resume

Cover Letter