Senior Medical Writer - Regulatory Documentation Lead
Listed on 2026-10-01
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Healthcare
Medical Science Liaison, Clinical Research, Healthcare Compliance
Parexel International is seeking an experienced Medical Writer to author and refine clinical documents for regulatory submissions, ensuring adherence to ICH-GCP guidelines and client SOPs.
The role involves project leadership, collaboration with cross-functional teams, and ensuring publishing readiness of final documents. Strong writing, editing, and communication skills are essential.
We have an opening for a Senior Medical Writer
- Regulatory Documentation Lead in United States within Marketing & Media, Bio & Pharmacology & Health.
Step into the Senior Medical Writer
- Regulatory Documentation Lead role at Parexel International in United States and grow with us.
Please review the full job details above before applying.
If your experience matches this role, we encourage you to apply.
All applications are reviewed carefully by our team.
This is a Full Time role.
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