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CSL is seeking a Senior Director, Head of Medical Writing, to lead a team responsible for the quality and delivery of clinical development documents. This hybrid role requires extensive experience in pharmaceutical clinical development and medical writing leadership, with a focus on collaboration and innovation.
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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.
CSL's R&D organization is accelerating innovation to deliver greater impact for patients.
Matching Summary
Match Score: 75
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CSL is seeking a Senior Director, Head of Medical Writing, to lead a team responsible for the quality and delivery of clinical development documents. This hybrid role requires extensive experience in pharmaceutical clinical development and medical writing leadership, with a focus on collaboration and innovation.
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Skills & Requirements
Must-have
clinical development documents
strategic CRO partners
recruiting, staffing and training
clinical development content
regulatory requirements
Quality Controls
enterprise initiatives
Nice-to-have
patient and health-care provider voice
culture of scientific integration
dynamic biotech ecosystems
meaningful difference worldwide
Key Requirements
Graduate level degree (M.Sc, PhD, MD etc)
10 yrs+ of Pharma experience
Experience across all phases of development
Experience across a wide range of regulatory document writing