Thoracic Oncology Clinical Development Executive Director

Pfizer

Bothell (WA)

Hybrid

USD 296,000 - 493,000

Full time

14 days+
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Benefits offered by this job

Relocation support

Job summary

Pfizer in the United States is seeking a Clinical Development Medical Executive Director to define and drive the development strategy for thoracic cancer programs. You will lead or support Global Development teams, integrate input from clinical, regulatory, and safety functions, and represent the program externally.

This role requires medical or advanced degree, 5+ years leading diverse teams, and late-phase development experience.

Qualifications

  • Medical degree or advanced degree with relevant clinical/industry experience (typically 5+ years).
  • Been licensed/registered by a medical licensing authority to prescribe medicines independent of Supervision for at least two years
  • 5+ years of experience leading diverse teams
  • Prior management responsibilities of medical directors or clinical scientists
  • Late phase drug development experience.

Responsibilities

  • May lead product specific Global Development Team (GDT)
  • Serves as the subject matter expert on clinical issues
  • Lead, develop and execute the clinical development plan of one or more indications in alignment with the Lifecycle Management Plan and Integrated Product Plan
  • Accountable for the clinical development strategy, trial design, execution, and delivery of trial results with the GDPL
  • Oversee the evaluation, interpretation, reporting and presentation of study data
  • Accountable with safety for clinical evaluations and safety decisions, escalating to GDPL as necessary

Skills

Leadership
Clinical trial leadership
Regulatory interactions
Strategic development

Education

Medical degree or advanced degree

Job description

Pfizer in the United States is seeking a Clinical Development Medical Executive Director to define and drive the development strategy for thoracic cancer programs. You will lead or support Global Development teams, integrate input from clinical, regulatory, and safety functions, and represent the program externally.

This role requires medical or advanced degree, 5+ years leading diverse teams, and late-phase development experience.

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