Scientific Director, Clinical Development, Respiratory

GlaxoSmithKline

Cambridge, MA, USA
Us base: $172,500 to $316,250; bonus/equity: annua...
Respiratory clinical research and development
Global clinical development program leadership
Clinical development strategy
Lead the clinical development strategy from a drug or program including accountability for the clinical components of the Target Medicine Profile (TMP) and leadership of the clinical matrix team (CMT)

Job Summary

  • Lead the clinical development strategy from a drug or program including accountability for the clinical components of the Target Medicine Profile (TMP) and leadership of the clinical matrix team (CMT).
  • Contribute to development of the Integrated Evidence Strategy (IES), including oversight of the CDP and its component clinical trials.
  • Manage technical and leadership development of Clinical Development staff via direct line management, mentoring and coaching across the organisation.

Matching Summary

Lead the clinical development strategy from a drug or program including accountability for the clinical components of the Target Medicine Profile (TMP) and leadership of the clinical matrix team (CMT).

Salary

US Base: $172,500 to $316,250; Bonus/Equity: Annual bonus and long-term incentive program; Benefits: Health care, retirement, paid time off

Skills & Requirements

Must-have

  • Respiratory clinical research and development
  • Global clinical development program leadership
  • Clinical development strategy
  • Clinical matrix team leadership
  • Global regulatory interactions
  • Risk/benefit assessment

Nice-to-have

  • Inspire and empower teams
  • Ambitious for patients
  • Accountable for impact
  • Uniting science, technology, and talent
  • Innovative methodologies and processes

Key Requirements

  • PhD or PharmD required
  • Experience in Respiratory clinical R&D
  • Experience leading global clinical development programs
  • Medical degree preferred
  • Proven track record leading cross-functional teams
  • In-depth knowledge of regulatory requirements and GCP
  • Experience with global regulatory agencies
  • Experience leading NDA, BLA, or MAA submissions

Work Rights

Not specified

Tailored Resume

Cover Letter