The Senior Medical Writer will lead the development of high-quality clinical study documents, including clinical study protocols, IBs, ICF templates, DSURs, CSRs, and CSR patient narratives.
Requirements
- Planning, writing, editing, formatting, and QC review of clinical documents
- Collaboration with Sponsor, external vendors, and internal project teams
- Ability to formulate key messages from clinical study data
- Excellent problem-solving skills
- Literature-based research to support writing activities
Benefits
- Discretionary annual bonus
- Health insurance
- Retirement savings benefits
- Life insurance
- Disability benefits
- Parental leave
- Paid time off for sick leave and vacation