Full-Time

Associate Principal Scientist

Safety Pharmacology

Confirmed live in the last 24 hours

MSD

MSD

Senior

H1B Sponsorship Available

North Wales, PA, USA

Hybrid work model requires three days in-office presence per week.

Category
Diagnostics & Laboratory Professionals
Physicians & Surgeons
Medical, Clinical & Veterinary
Requirements
  • PhD with 6+ years relevant post-degree experience in the development, execution and interpretation of in vitro exploratory or regulated nonclinical safety pharmacology/toxicology models.
  • Ability to work both within teams as a contributor or as a team lead to drive collaborations across departments that deliver current needs and future capabilities.
  • Experience in ion channel electrophysiology and its practical applications to standard screening and investigative models (ex: over-expressing cells, semi-automated platforms) to drive off target screening or enhanced mechanistic understanding of effects of major organ systems.
  • Development and/or utilization of exploratory hIPSC-derived models (plate-based or 'organ-on-a-chip')- or microphysiologic systems to enable issue-driven resolution and complement preclinical candidate selection and development.
  • Experience either as a study director or contributing scientist for studies conducted under Good Laboratory Practices (GLP) that utilize common nonclinical in vitro test systems (e.g., best practice in vitro studies outlined in ICH E14 / S7B Q&A).
  • Hands-on experience on patch clamp techniques and/or utilizing microelectrode arrays, impedance or imaging as readouts.
  • Willingness and ability to investigate, develop and implement new technologies and capabilities to improve existing techniques and assays.
  • Prior experience working in a multidisciplinary environment within the Pharmaceutical Industry, Regulatory Agencies, or Academic Institutions.
  • Willingness to influence safety pharmacology science and the broader regulatory landscape through active participation in external consortiums, publications, and presentations at key scientific conferences.
  • Experience or familiarity with biostatistics, programming, and/or data visualization tools.
  • Experience in other safety pharmacology core areas (e.g., in vitro neuronal models to assess hyperexcitability risks)
Responsibilities
  • Complement existing areas, expand the team’s expertise, help drive future innovation, and influence the external scientific and regulatory community.
  • Drive collaborations across departments that deliver current needs and future capabilities.

Company Stage

N/A

Total Funding

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Headquarters

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Founded

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