GSK·17 days ago
17 days ago
Director Medical Writing Asset Lead
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What you'll do
- Shape clinical document strategy and accelerate product approvals for GSK’s Hepatology assets
- Lead high-quality submissions
- Collaborate across teams
- Drive process improvements
What they're looking for
- Experienced medical writers with strong leadership and regulatory writing expertise
Summarised by NextRaise from the employer’s description, which follows in full below.
Full description from employer
We are looking for a Director Medical Writing Asset Lead to shape clinical document strategy and accelerate product approvals for GSK’s Hepatology assets. Lead high-quality submissions, collaborate across teams, and drive process improvements. Ideal for experienced medical writers with strong leadership and regulatory writing expertise.
Skills
- clinical regulatory writing
- clinical trial design
- ich-gcp compliance
- project management
- submission planning
- pharmaceutical industry
- learning agility
- decision making
- regulatory submissions
- clinical trial designs
- medical writing
- influencing without authority
- strategic thinking
- customer service
- presentation techniques
- clinical development
- literature reviews
- emotional intelligence
- scientific writing
- communication
- matrix leadership
- clinical document development
- stakeholder management
- process improvement
- training material development
- mentoring
- cross-functional collaboration
- problem solving
Company
GSK
Bengaluru, India
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