Technical Writer (GLP Studies – Product Safety Labs)

About the role

The Technical Writer supports the preparation, revision, formatting, control, and organization of study documentation associated with GLP-compliant preclinical research. The role enables Study Directors to focus on scientific interpretation and regulatory accountability.

What you'll do

• Prepare first drafts of study protocols using approved templates and Study Director guidance
• Coordinate the development, review, revision, and issuance of study protocols, amendments
• Prepare report sections, narratives, tables, and appendices from approved source data
• Create shell reports, templates, and standardized study documents
• Coordinate document review cycles, comment resolution, and final issuance

What you need

• 4–6 yrs of experience
• GLP
• Writing
• Technical writing
• Editing
• CRO
• Proofreading
• Any graduate