Global Development Lead, Internal Medicine (md, Sr. Director)

Pfizer

Multiple Locations
Base: $274,500.00 - $457,500.00; bonus/equity: 25....
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Clinical development plan
Protocol design documents
Worldwide regulatory submissions
** Pfizer is seeking a Global Development Lead for Internal Medicine (Sr. Director) who will oversee clinical development for assigned assets. The ideal candidate should have significant experience in clinical research and development, particularly within the biopharmaceutical industry. **

Job Summary

  • The Global Development Lead represents Clinical on the Global Medicine Team and is the single clinical point of accountability for clinical development for assigned asset(s) in Internal Medicine.
  • Responsibilities include creating and gaining endorsement for the Clinical Development Plan, leading cross-functional teams, and partnering with other clinical and operations colleagues throughout the lifecycle of studies.
  • The role requires an MD or DO with 8+ years of relevant experience, extensive knowledge of clinical development, global and regional regulation, and demonstrated leadership capabilities.

Matching Summary

Match Score: 75

** Pfizer is seeking a Global Development Lead for Internal Medicine (Sr. Director) who will oversee clinical development for assigned assets. The ideal candidate should have significant experience in clinical research and development, particularly within the biopharmaceutical industry. **

Salary

Base: $274,500.00 - $457,500.00; Bonus/Equity: 25.0% bonus target; Benefits: Comprehensive and generous benefits

Skills & Requirements

Must-have

  • Clinical development plan
  • Protocol design documents
  • Worldwide regulatory submissions
  • Clinical pharmacology
  • Statistics
  • Safety
  • Commercial
  • Patient access
  • Operations
  • Therapeutic area expertise
  • Global development programs
  • ICH/GCP
  • Adverse event management

Nice-to-have

  • Innovative thinking
  • Bold decision making
  • Digital/innovation approaches
  • Patient engagement approaches
  • External stakeholder engagement
  • Product label development

Key Requirements

  • MD or DO
  • 8+ years of experience
  • Cardiologist with cardiovascular outcome trials experience
  • Extensive knowledge of clinical development
  • Global and regional regulation
  • ICH/GCP
  • Adverse event management
  • Demonstrated clinical/medical, administrative, and project management capabilities
  • Demonstrated experience managing and training large teams
  • Demonstrated experience in designing and launching large teams preferred

Work Rights

Permanent work authorization required

Tailored Resume

Cover Letter