At GSK, we are seeking a Director Medical Writing Asset Lead, Oncology to lead medical writing for one or more development oncology assets, with accountability for asset-level medical writing strategy from planning to delivery.
Requirements
- Postgraduate degree e.g. PhD, PharmD, MSc, MPH, in life sciences, pharmacy, medicine, public health or related discipline
- Significant experience in clinical regulatory medical writing within the pharmaceutical or biotech industry
- Experience in authoring and leading regulatory clinical documents for global oncology FDA and/or EMA submissions
- Experience in leading multi-disciplinary, matrix teams and managing external medical writing vendors
- Experience in program management i.e. project planning and delivery skills, including risk identification and timeline management
- Written and verbal communication skills with the ability to present complex scientific content clearly.
Benefits
- Private healthcare
- Additional paid days off
- Life insurance
- Private pension plan
- Fully paid parental leave & care of family member leave