SGS · Richardson, TX

Clinical Writer I at SGS — Richardson, TX

Full-timeRichardson, TXPosted 2026-07-22Apply on SmartRecruiters
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Full job description

  • Drafts protocols and reports for clinical studies on cosmetics or other claims.
  • Uses internal or client template, study outline, clinical data, International Council on Harmonisation (ICH) and Good Clinical Practice (GCP) guidelines, and other relevant information.
  • Coordinates internal and external protocol reviews and obtains client agreement
  • Writes and reviews ICH/GCP-adherent clinical study protocols, coordinates internal and external reviews, and obtains client agreement by project deadline
  • Drafts clinical study reports based on internal or client template according to clinical data, protocol and amendments and deviations; revises reports based on reviews by quality assurance, statistics department, investigators, client, and others
  • Assists in maintaining internal databases of protocol and report templates, bioinstrumentation specifications, clinical grading parameters, and client preferences
  • Assists in drafting and editing Standard Operating Procedures (SOPs) and Work Instructions (WI) for department as assigned
  • Completes training within required deadline
  • Adheres to internal standards, policies, and procedures
  • Bachelor’s degree (technical writing, English, or science preferred).
  • 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)
  • Microsoft Excel: Intermediate proficiency