Similar Jobs
See allPrincipal Medical Writer
Veristat
US
Medical Writing
Regulatory Documentation
ICH Guidelines
Senior Medical Writer/Principal Medical Writer
Precision Medicine Group
UK
Medical Writing
Microsoft Office
Clinical Research
Senior/Principal Medical Writer
Jobgether
Europe
Medical Writing
Regulatory Documentation
Project Management
Senior Medical Writer
Avalere Health
US
Medical Writing
Scientific Communication
MS Office
Medical Director - Market Access Marketing
PRECISION AQ
United States
Content Development
Medical Writing
Regulatory Compliance
About the Role:
- The Principal Medical Writer independently plans and prepares regulatory documents and medical communications to support all phases of product development.
- This role involves organizing, analyzing, interpreting, and presenting scientific and statistical information in accordance with ICH guidelines.
What You'll Do:
- Organize, analyze, interpret, and present scientific and statistical information per ICH and other regulatory guidelines.
- Collaborate with cross-functional internal and external document production teams.
- Work under the direction of Medical Writing management.
What We're Looking For:
- Bachelor's degree in a science-related field with at least 7 years of medical writing experience in a CRO or pharmaceutical setting.
- Advanced knowledge of ICH and regulatory guidelines, excellent written English, and keen attention to detail.
- Proficiency in Microsoft Office Suite, including advanced Microsoft Word skills.
What We Offer:
- Remote working with flexible time off and paid holidays.
- Medical insurance, tuition reimbursement, and retirement plans.
- A diverse and inclusive culture with a global team.
Veristat
Veristat is a global contract research organization with over 30 years of expertise accelerating life-changing therapies to patients worldwide. The company has a flexible, inclusive culture with a 70% remote workforce and 66% women-led teams.