Senior Director, Quantitative Pharmacology - PK/PD Strategy

Otsuka Pharmaceutical Co., Ltd.

United States

Presencial

USD 231.000 - 345.000

Jornada completa

14 días+

Una candidatura completa en un minuto

Currículum y carta de presentación personalizados, listos para enviar.

Supera los filtros ATS

Ventajas ofrecidas por este puesto de trabajo

Comprehensive medical, dental, vision,
401(k) with match
Tuition reimbursement

Descripción de la vacante

Otsuka Pharmaceutical Co., Ltd. seeks a Clinical Pharmacology Lead within the Quantitative Pharmacology group (QTR) to guide drug development through PK/PD strategy, dose selection, and regulatory support.

You will mentor scientists, shape SOPs, and partner with cross-functional teams to advance early- to late-stage programs. You will oversee pre-IND through phase 3 activities, review PK/PD analyses, and help translate data into actionable development plans.

Formación

  • PhD in Clinical Pharmacology (or related) with 12+ years in the field.
  • Experience in early-phase protocol development is a plus.
  • Extensive experience developing and executing clinical pharmacology strategies.
  • Strong leadership and mentoring abilities.

Responsabilidades

  • Lead clinical pharmacology strategy across all development stages.
  • Oversee PK/PD reports and regulatory submissions.
  • Mentor junior scientists in Quantitative Pharmacology.
  • Collaborate with cross-functional teams (toxicology, DMPK, biomarker, bioanalytical).
  • Develop SOPs and cross-functional working processes.
  • Interact with BD opportunities and go/no-go decisions.

Conocimientos

Leadership
Communication skills
Adaptability
Organizational skills
Scientific knowledge application

Educación

PhD in Clinical Pharmacology

Herramientas

Phoenix NLME

Descripción del empleo

Otsuka Pharmaceutical Co., Ltd. seeks a Clinical Pharmacology Lead within the Quantitative Pharmacology group (QTR) to guide drug development through PK/PD strategy, dose selection, and regulatory support.

You will mentor scientists, shape SOPs, and partner with cross-functional teams to advance early- to late-stage programs. You will oversee pre-IND through phase 3 activities, review PK/PD analyses, and help translate data into actionable development plans.

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