Scientific Technical Writer - GLP/ICH Docs Specialist

Downtown Boulder Partnership; Cincinnati (OH); On-site; USD 65,000 - 90,000; Full time

Job summary

Medpace in Cincinnati, OH is seeking a Scientific Technical Writer to support scientists by preparing protocols, methods, and sponsor study reports, and to organize study notebooks and related documents.

The position requires a Bachelor’s degree, prior experience in a research laboratory, and strong written and oral communication skills. Knowledge of GLP, cGMP, and ICH guidelines, and proficiency with Microsoft Word, Excel, and PowerPoint are essential.

Qualifications

• Bachelor’s degree required.
• Previous experience in a research laboratory.
• Strong written and oral communication skills.
• Knowledge of GLP, cGMP, and ICH guidelines.
• Proficiency with Word, Excel, and PowerPoint.

Responsibilities

• Assist scientists in preparing protocols, methods, and reports for sponsor studies.
• Organize study documents such as notebooks, sample receiving documents, CoAs of reference standards, etc., for individual studies.
• Compile and review results from instruments and the Watson‑LIMS database for report writing.
• Use templates to prepare protocols and reports efficiently.

Skills

Strong written and oral communication

GLP, cGMP, and ICH knowledge

Microsoft Word

Microsoft Excel

Microsoft PowerPoint

Education

Bachelor's degree

Tools

Microsoft Word

Microsoft Excel

Microsoft PowerPoint

Job description

Medpace in Cincinnati, OH is seeking a Scientific Technical Writer to support scientists by preparing protocols, methods, and sponsor study reports, and to organize study notebooks and related documents.

The position requires a Bachelor’s degree, prior experience in a research laboratory, and strong written and oral communication skills. Knowledge of GLP, cGMP, and ICH guidelines, and proficiency with Microsoft Word, Excel, and PowerPoint are essential.