Scientific Leader, In Vivo Pharmacology

GSK

Cambridge, Massachusetts, United States
Base: $140,250 to $233,750; bonus/equity: annual b...
In vivo pk/pd study design
Rodent and non-human primate models
Oligonucleotide therapeutics
The individual will be involved in designing and executing PK/PD studies supporting the advancement of oligonucleotide therapeutics

Job Summary

  • The individual will be involved in designing and executing PK/PD studies supporting the advancement of oligonucleotide therapeutics.
  • Manage and oversee in vivo studies conducted internally or with external CRO, including scope definition, protocol review, operational activities, data quality oversight, and scientific interpretation and communication of results.
  • Available benefits include health care and other insurance benefits (for employee and family), retirement benefits, paid holidays, vacation, and paid caregiver/parental and medical leave.

Matching Summary

The individual will be involved in designing and executing PK/PD studies supporting the advancement of oligonucleotide therapeutics.

Salary

Base: $140,250 to $233,750; Bonus/Equity: annual bonus and long term incentive program; Benefits: health care, retirement, paid holidays, vacation, leave

Skills & Requirements

Must-have

  • in vivo PK/PD study design
  • rodent and non-human primate models
  • oligonucleotide therapeutics
  • molecular biology assays
  • qPCR assay development and execution

Nice-to-have

  • operational excellence
  • scientific expertise
  • cross-functional collaboration
  • risk mitigation strategies
  • ambitious for patients

Key Requirements

  • PhD in Pharmacology, Biology, Biochemistry, or related
  • 4+ years relevant industry experience
  • 3+ years in vivo PK/PD study design and execution
  • 2+ years working with oligonucleotide therapeutics
  • 3+ years independently designing studies
  • 3+ years conducting in vivo techniques

Work Rights

Not specified

Tailored Resume

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