Director Medical Writing Asset Lead

As Medical Writing Asset Lead Director, you will provide medical writing strategy for one or more assets, design and deliver high-quality clinical documents for global regulatory submissions, and contribute to organizational process improvements. You will balance scientific rigor with practical execution, champion efficient and accelerated ways of working, and proactively identify opportunities to simplify document lifecycle, reduce risk and strengthen submission quality across the asset lifecycle.

Requirements

• Postgraduate degree in life sciences, pharmacy, medicine, public health or related discipline
• Extensive experience in clinical regulatory writing in the pharmaceutical industry
• Experience in project management, planning, communication, and demonstrated matrix leadership to deliver results
• Excellent understanding of clinical operations / medical writing processes, and ICH/GCP and global regulatory guidelines for drug development and approval
• Strong strategic and critical thinking, problem solving, influencing and decision-making capabilities

Benefits

• Private healthcare
• Additional paid days off
• Life insurance
• Private pension plan
• Fully paid parental leave & care of family member leave