Senior Director, Head Of Medical Writing

CSL

King of Prussia, PA, USA
Hybrid (onsite three days a week)
Clinical development documents
Strategic cro partners
Recruiting, staffing, training
CSL is seeking a Senior Director, Head of Medical Writing to lead their medical writing team and ensure the quality of clinical development documents. This hybrid role requires extensive experience in pharmaceutical clinical development and a strong leadership background, with a focus on collaboration and innovation

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: 85

CSL is seeking a Senior Director, Head of Medical Writing to lead their medical writing team and ensure the quality of clinical development documents. This hybrid role requires extensive experience in pharmaceutical clinical development and a strong leadership background, with a focus on collaboration and innovation.

Skills & Requirements

Must-have

  • clinical development documents
  • strategic CRO partners
  • recruiting, staffing, training
  • high-quality clinical content
  • regulatory requirements
  • submission plans
  • publications support
  • Quality Controls
  • processes and templates
  • incorporating technologies
  • enterprise initiatives
  • scientific integration
  • patient and health-care provider voice

Nice-to-have

  • dynamic biotech ecosystems
  • agile team
  • future-ready team
  • meaningful difference worldwide
  • cutting-edge scientific expertise
  • consistent product messaging strategy
  • compelling fashion
  • accuracy and consistency
  • enhanced organizational awareness
  • culture of urgency, quality, innovation
  • peer review
  • Inclusion and Belonging

Key Requirements

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

Work Rights

Not specified

Tailored Resume

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