Senior Pharmacovigilance Scientist, Global Safety Strategy

Merck & Co.

North Wales (Montgomery County)

Híbrido

USD 232 000 - 365 000

Tempo integral

14 dias+

Uma candidatura completa num minuto

Currículo e carta de apresentação personalizados, prontos a enviar.

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Vantagens oferecidas por esta oferta de emprego

Medical, dental, vision benefits
401(k) and retirement benefits
Paid holidays and vacation

Resumo da oferta

Merck & Co. is seeking a CSRM Physician, Principal Scientist to lead clinical risk management and safety surveillance for investigational and marketed products.

This physician will chair the RMST, integrate safety strategies across Clinical Development, Epidemiology, Regulatory Affairs, Biostatistics, and Manufacturing, and guide safety assessments throughout the product lifecycle. Ideal candidates hold an MD/DO with board certification (preferred), have at least 3 years of clinical experience,

Qualificações

  • MD/DO or equivalent medical degree required.
  • Board certification preferred for clinical leadership tracks.
  • Strong written and verbal communication skills; ability to lead cross-functional teams.

Responsabilidades

  • Lead risk management and pharmacovigilance plans for assigned products.
  • Chair RMST and partner with Clinical Development and Regulatory groups.
  • Ensure robust safety surveillance across product lifecycle and prepare regulatory submissions.

Conhecimentos

Clinical Risk Mgmt
Clinical Safety
Pharmacovigilance
Safety Strategy
Medical Writing
Regulatory Submissions
Cross-Functional Leadership

Formação académica

MD/DO or equivalent
Board Certification (preferred)

Descrição da oferta de emprego

Merck & Co. is seeking a CSRM Physician, Principal Scientist to lead clinical risk management and safety surveillance for investigational and marketed products.

This physician will chair the RMST, integrate safety strategies across Clinical Development, Epidemiology, Regulatory Affairs, Biostatistics, and Manufacturing, and guide safety assessments throughout the product lifecycle. Ideal candidates hold an MD/DO with board certification (preferred), have at least 3 years of clinical experience,

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