Bioanalysis Leader & Scientific Director – GLP Expert

Charles River

Reno (NV)

Presencial

USD 145 000 - 150 000

Tempo integral

14 dias+

Uma candidatura completa num minuto

Currículo e carta de apresentação personalizados, prontos a enviar.

Ultrapassa os filtros ATS

Vantagens oferecidas por esta oferta de emprego

Bonus/incentives
401K
Paid time off
Health and wellness coverage

Resumo da oferta

Charles River is seeking a senior scientific leader to oversee discovery through regulated GLP and clinical bioanalytical services. You will manage scientific staff, provide direction and mentorship, and maintain strong sponsor relationships while ensuring regulatory compliance of procedures and data management.

This role requires a PhD, 10+ years in contract research or pharma, GLP experience, and proven leadership.

Qualificações

  • PhD or international equivalent in a science-related field required.
  • 10+ years in contract research or pharmaceutical industry conducting scientific research.
  • GLP discovery environment experience and proven management ability.
  • Strong communication, analytical and leadership skills.

Responsabilidades

  • Provide scientific direction and oversight for discovery through GLP and clinical bioanalytical services.
  • Mentor junior staff and manage assigned scientific personnel.
  • Develop and maintain sponsor relationships and participate in business development.
  • Ensure regulatory compliance of lab procedures, documentation, and data management.
  • Lead implementation of new procedures and cross-functional collaboration.

Conhecimentos

Leadership
Supervisory experience
Communication
Project management
Analytical thinking

Formação académica

PhD or international equivalent in science

Ferramentas

MS Word
MS Excel
Outlook

Descrição da oferta de emprego

Charles River is seeking a senior scientific leader to oversee discovery through regulated GLP and clinical bioanalytical services. You will manage scientific staff, provide direction and mentorship, and maintain strong sponsor relationships while ensuring regulatory compliance of procedures and data management.

This role requires a PhD, 10+ years in contract research or pharma, GLP experience, and proven leadership.

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