Clinical Protocol & Report Writer I

SGS; Richardson (TX); On-site; USD 65,000 - 90,000; Full time

Job summary

SGS in Richardson, TX is seeking a technical writer to draft protocols and reports for clinical studies on cosmetics or other claims, ensuring alignment with ICH and GCP guidelines.

You will coordinate internal and external protocol reviews, maintain templates and SOPs, and draft reports revised by QA, statistics, investigators and clients. Strong editing, organizational and research skills are essential.

Qualifications

• Bachelor’s degree in technical writing, English, or science.
• 0-4 years technical writing experience.
• Strong technical writing and editing skills including internal document consistency.
• Organizational ability, research skills, attention to detail, and the ability to establish priorities with minimal supervision.
• Microsoft Word: Intermediate proficiency (including table creation).

Responsibilities

• Drafts protocols and reports for clinical studies on cosmetics or other claims.
• Uses internal or client templates, study outlines, clinical data, ICH and GCP guidelines.
• Coordinates protocol reviews and obtains client agreement.
• Writes and reviews ICH/GCP-adherent protocols and coordinates reviews.
• Drafts clinical study reports and revises them after QA and client feedback.
• Assists in maintaining internal databases of templates and SOPs.

Skills

Technical writing

Editing

Attention to detail

Research skills

Education

Bachelor's degree in technical writing, English, or science

Tools

Microsoft Word

Job description

SGS in Richardson, TX is seeking a technical writer to draft protocols and reports for clinical studies on cosmetics or other claims, ensuring alignment with ICH and GCP guidelines.

You will coordinate internal and external protocol reviews, maintain templates and SOPs, and draft reports revised by QA, statistics, investigators and clients. Strong editing, organizational and research skills are essential.