The Senior Medical Writer will lead the development of high-quality clinical study documents, including clinical study protocols, IBs, ICF templates, DSURs, CSRs, CSR patient narratives, and ensure smooth and effective document management from start to finish.
Requirements
- Planning, writing, editing, formatting, and QC review of clinical documents
- Collaboration with Sponsor, external vendors, and/or internal Precision project teams/departments
- Ability to author complex content using knowledge/skills and understanding of processes
- Excellent problem-solving skills
- Performing 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