A biotechnology company is seeking a new Medical Writer to join their team, managing technical quality control and project management activities to support aggregate safety reporting.
**This is a Remote opportunity.***
Responsibilities:
- Leading project management for various aggregate deliverables
- Maintaining reporting calendars and tracking milestones
- Ensuring on-time, inspection-ready reports
- Writing key sections of ASRs and related documents
- Performing QC to ensure accuracy and compliance
- Performing other duties, as needed
Qualifications:
- 3+ years of Medical Writing or related experience
- Bachelor’s degree in a relevant field
- Experience with regulatory documentation and processes
- Strong organizational skills
- Attention to detail
- Proven ability to manage multiple projects
- Effective communication skills
Desired Skills:
- 5+ years of Medical Writing or related experience
- Advanced Degree in life sciences or related area
- PMP or similar certification
- Certifications in Project Management or Medical Writing
