Senior Clinical Development Scientist (Hybrid)

Pfizer Inc

United States

Híbrido

USD 139 000 - 232 000

Tempo integral

Há 2 dias
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Vantagens oferecidas por esta oferta de emprego

Relocation support
Hybrid work model
Comprehensive benefits

Resumo da oferta

Pfizer Inc. is seeking a Clinical Development Scientist (Senior Manager) in a hybrid US role to provide clinical oversight across Internal Medicine trials.

You will influence protocol design, safety reviews, data integrity, and regulatory submissions while mentoring team members and coordinating with investigators and health authorities. The position requires a science degree with range of clinical research experience.

Qualificações

  • Science degree or higher with clinical research experience
  • Experience in protocol development, SOPs, and regulatory submissions
  • Ability to lead cross-functional teams and mentor others
  • Strong communication with investigators, KOLs and health authorities
  • Knowledge of ICH/GCP and clinical development lifecycle

Responsabilidades

  • Provide clinical oversight for one or more studies and deliverables
  • Contribute to protocol development and amendments
  • Support governance submissions and regulatory interactions
  • Develop informed consent documents and safety narratives
  • Review SAPs, CRFs, and data review plans for data quality
  • Support TMF compliance and regulatory filings and audits

Conhecimentos

Clinical leadership
Regulatory knowledge
Study design input
Mentoring/coaching
KOL/Health Authority interactions
Data review & safety monitoring
Communication skills
Experience with AI tools

Formação académica

Science degree (PhD, PharmD, or equivalent)
MA/MS with 5+ years clinical research
BA/BS with 6+ years clinical research

Ferramentas

AI tools

Descrição da oferta de emprego

Pfizer Inc. is seeking a Clinical Development Scientist (Senior Manager) in a hybrid US role to provide clinical oversight across Internal Medicine trials.

You will influence protocol design, safety reviews, data integrity, and regulatory submissions while mentoring team members and coordinating with investigators and health authorities. The position requires a science degree with range of clinical research experience.

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