Senior Director, Head Of Medical Writing

CSL

King of Prussia, PA, USA
**
Clinical development documents
Strategic cro partners
Recruiting and training medical writers
** CSL is seeking a Senior Director, Head of Medical Writing, to lead a team responsible for creating high-quality clinical development documents. This hybrid position requires extensive experience in the pharmaceutical industry, particularly in clinical writing and leadership, to enhance collaboration and innovation in medical writing. **

Job Summary

  • The incumbent will be responsible for the quality and delivery of high-quality clinical development documents across the portfolio in collaboration with strategic CRO partners.
  • Responsible for overseeing the recruiting, staffing and training development of the medical writing specialists in the group.
  • Develop a strategy for incorporating technologies to enhance and improve delivery of medical writing content (eg, AI tools).

Matching Summary

Match Score: 75

** CSL is seeking a Senior Director, Head of Medical Writing, to lead a team responsible for creating high-quality clinical development documents. This hybrid position requires extensive experience in the pharmaceutical industry, particularly in clinical writing and leadership, to enhance collaboration and innovation in medical writing. **

Skills & Requirements

Must-have

  • clinical development documents
  • strategic CRO partners
  • recruiting and training medical writers
  • clinical safety and regulatory requirements
  • messaging strategy across a program
  • Quality Controls for documents
  • incorporating technologies for medical writing

Nice-to-have

  • patient and health-care provider voice integration
  • culture of urgency and quality
  • enhancing company reputation externally
  • collaboration with partnering functions

Key Requirements

  • Graduate level degree (M.Sc, PhD, MD etc)
  • 10 yrs+ of Pharma experience
  • Experience across all phases of development
  • Track record of successful medical writing leadership
  • Experience across a wide range of regulatory document writing
  • Extensive experience of leading teams

Work Rights

Not specified

Tailored Resume

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