Regulatory Affairs Strategist for AI-Document Tasks (Remote)

Ethos; Singapore; On-site; SGD 33,000 - 133,000; Part time

Job summary

Ethos is recruiting remote regulatory affairs specialists to help train AI models on professional documents, spreadsheets, and slide decks. The role emphasizes authoring and reviewing clinical study reports, protocol synopses, and regulatory dossier modules with strict adherence to ICH-GCP guidelines.

The hour rate is $100 with flexible commitment of 5–20 hours per week, offering fully remote work and ASAP start.

Qualifications

• Direct experience authoring or reviewing CSR, protocol synopses, or regulatory dossier modules.
• Deep familiarity with ICH-GCP standards, FDA/EMA regulatory expectations.
• Excellent written communication and attention to detail in documents.

Responsibilities

• Create, evaluate, and refine AI-generated regulatory documents across CSRs, protocols, investigator brochures, and dossier modules.
• Ensure scientific rigor and regulatory compliance in AI-assisted outputs.
• Collaborate with Ethos and AI lab teams to optimize workflows and document quality.

Skills

Regulatory affairs expertise

CSR/protocol documentation

Scientific writing

Job description

Ethos is recruiting remote regulatory affairs specialists to help train AI models on professional documents, spreadsheets, and slide decks. The role emphasizes authoring and reviewing clinical study reports, protocol synopses, and regulatory dossier modules with strict adherence to ICH-GCP guidelines.

The hour rate is $100 with flexible commitment of 5–20 hours per week, offering fully remote work and ASAP start.