Director Clinical Development Scientist, Early Clinical Development

pfizer.ca

Base: $176,600.00 to $294,300.00; bonus/equity: 20...
Hybrid
Lead clinical protocol development
Execute clinical studies
Safety assessment and interpretation
Lead and coordinate the development and execution of multiple studies for small molecule and/or novel biological therapies, spanning from first in human (FIH), proof of mechanism (PoM), early signals of efficacy (ESoE) and proof of concept (PoC) studies

Job Summary

  • Lead and coordinate the development and execution of multiple studies for small molecule and/or novel biological therapies, spanning from first in human (FIH), proof of mechanism (PoM), early signals of efficacy (ESoE) and proof of concept (PoC) studies.
  • Independently lead the development of the clinical protocol and participate as an individual contributor on clinical study teams to meet enrollment and study delivery timelines.
  • The annual base salary for this position ranges from $176,600.00 to $294,300.00, with eligibility for a bonus target of 20.0% and long-term incentives.

Matching Summary

Lead and coordinate the development and execution of multiple studies for small molecule and/or novel biological therapies, spanning from first in human (FIH), proof of mechanism (PoM), early signals of efficacy (ESoE) and proof of concept (PoC) studies.

Salary

Base: $176,600.00 to $294,300.00; Bonus/Equity: 20.0% bonus target and long-term incentives; Benefits: Comprehensive benefits including 401(k), vacation, paid leave, health benefits

Skills & Requirements

Must-have

  • Lead clinical protocol development
  • Execute clinical studies
  • Safety assessment and interpretation
  • Clinical data review strategy
  • Scientific and clinical literature knowledge
  • Good clinical practice (GCP) compliance

Nice-to-have

  • Influence and collaborate with peers
  • Develop and coach others
  • Build consensus and drive change
  • Establish external expert relationships

Key Requirements

  • MD/BS/BA/BSN and 8+ years experience
  • MS/MA/MSN and 7+ years experience
  • PhD/PharmD and 5+ years experience
  • 3-5 years in a clinician type role
  • Understanding of biopharmaceutical environment
  • Proven scientific writing skills
  • Strong communication/interpersonal skills

Work Rights

Permanent work authorization in the United States

Tailored Resume

Cover Letter