Regulatory Writer for Life Sciences
1 day ago
We are looking for a skilled medical writer to join our team at Harvest Technical Services, Inc.
Main Responsibilities- Drafts and edits clinical study protocols, informed consent forms, and other regulatory documents.
- Collaborates with cross-functional teams to develop and manage timelines for document preparation.
- Ensures adherence to technical and industry standards, maintaining high-quality document production.
- Bachelor's or higher degree in a scientific field.
- At least 5 years of experience in medical writing, with expertise in protocol development and clinical study reports.
- Familiarity with the drug development process and regulatory requirements is essential.
$45 to $53 per hour, based on internal equity and market conditions.
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Life Sciences Medical Writer Position
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