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Senior CMC Regulatory Affairs Professional
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Medical Writer, Medical Communications
Precision Medicine Group
US
Microsoft Word
PowerPoint
Excel
Accountabilities:
- Lead the preparation and review of clinical study reports, protocols, and other regulatory documents to ensure accuracy and clarity.
- Perform medical writing tasks of high complexity and critical importance to ongoing projects.
- Develop clinical trial reports (CTRs) and lay summaries of clinical trial results.
Requirements:
- Advanced degree in life sciences, medicine, or a related field; relevant certifications preferred.
- Minimum 5 years of experience as a regulatory medical writer.
- Strong understanding of regulatory requirements and industry standards.
Why Apply:
- Competitive salary and diverse culture that rewards high performance.
- Various annual leave entitlements.
- Opportunities for ongoing learning and career development.
Jobgether
Jobgether uses an AI-powered matching process to ensure your application is reviewed quickly, objectively, and fairly against the role's core requirements. They identify the top-fitting candidates, and this shortlist is then shared directly with the hiring company.