Scientific Technical Writer: GLP/cGMP Protocols & Reports

Medpace; Cincinnati (OH); On-site; USD 65,000 - 85,000; Full time

Job summary

Medpace is seeking a full-time, office-based Scientific Technical Writer in Cincinnati, Ohio. You will work with scientists to prepare protocols, methods, and reports for sponsor studies, organize study documents, and compile results from instruments and Watson-LIMS for report writing.

The role emphasizes strong writing and communication skills, familiarity with GLP, cGMP, and ICH guidelines, and proficiency with Microsoft Word, Excel, and PowerPoint. Travel is None.

Qualifications

• Bachelor's degree with laboratory experience.
• Willingness to write and strong writing communication skills.
• Knowledge of GLP, cGMP, and ICH guidelines.
• Strong organizational and written/oral communication skills.
• Proficiency with Microsoft Word, Excel, and PowerPoint.

Responsibilities

• Assist scientists to prepare protocols, methods and reports for sponsors' studies.
• Organize study documents such as notebooks, sample receiving documents, CoAs of reference standards for individual studies.
• Compile and review results from instruments and Watson-LIMS for report writing.
• Able to use templates to prepare protocols and reports for scientists efficiently.

Skills

Writing

Communication

Organizational skills

MS Word

MS Excel

MS PowerPoint

Education

Bachelor's degree

Tools

Watson-LIMS

Job description

Medpace is seeking a full-time, office-based Scientific Technical Writer in Cincinnati, Ohio. You will work with scientists to prepare protocols, methods, and reports for sponsor studies, organize study documents, and compile results from instruments and Watson-LIMS for report writing.

The role emphasizes strong writing and communication skills, familiarity with GLP, cGMP, and ICH guidelines, and proficiency with Microsoft Word, Excel, and PowerPoint. Travel is None.