Remote Pharma AI Documentation Consultant

Ethos; Dubai; On-site; AED 430,000 - 582,000; Part time

Benefits offered by this job

Remote work

Flexible schedule

Job summary

Ethos is seeking pharma and clinical development professionals with 5+ years of experience to help train an AI model on professional documents, spreadsheets, and slide decks across core workflows such as clinical study reports, protocol synopses, investigator brochures, and regulatory dossiers.

The role is fully remote with flexible, 5–20 hours per week and an ASAP start date. You will craft, review, and refine high-quality materials with strict adherence to ICH-GCP and regulatory expectations.

Qualifications

• Direct experience authoring or reviewing clinical study reports, protocol synopses, or regulatory dossier modules for a pharmaceutical, biotech, or CRO organization
• Deep familiarity with ICH-GCP standards, FDA/EMA regulatory expectations, and the scientific rigor required in investigator brochures and medical affairs materials
• Expert-level document, spreadsheet, and slide craftsmanship, with excellent written communication and attention to detail

Responsibilities

• Create, evaluate, and refine AI-generated pharma documents, spreadsheets, and slide decks across core workflows (clinical study reports, protocol synopses, investigator brochures, regulatory dossier modules, medical affairs slide decks, and publication plans)
• Ensure compliance with ICH-GCP standards and regulatory expectations in all materials
• Collaborate with sponsors to polish clinical study materials for regulatory submissions and publications

Skills

Clinical study reports

Protocol synopses

Regulatory dossiers

Job description

Ethos is seeking pharma and clinical development professionals with 5+ years of experience to help train an AI model on professional documents, spreadsheets, and slide decks across core workflows such as clinical study reports, protocol synopses, investigator brochures, and regulatory dossiers.

The role is fully remote with flexible, 5–20 hours per week and an ASAP start date. You will craft, review, and refine high-quality materials with strict adherence to ICH-GCP and regulatory expectations.