Remote Clinical Research Associate — AI Document & Deck Specialist

Ethos; Singapore; On-site; SGD 149,000 - 202,000; Full time

Job summary

Ethos is partnering with a leading AI-focused lab to engage experienced clinical research associates. You will author, review, and refine AI-assisted clinical documents, including study reports and regulatory materials, maintaining high scientific rigor.

Applicants should have 5+ years in clinical research or regulatory affairs and deliver precise, well-structured documents for flexible, remote, part-time work at.$100/hour, ASAP 시작.

Qualifications

• Direct experience authoring or reviewing CSR, protocol synopses, or regulatory dossier modules.
• Deep familiarity with ICH-GCP standards, FDA/EMA regulatory expectations.
• Expert-level document, spreadsheet, and slide craftsmanship with strong written communication.

Responsibilities

• Create, evaluate, and refine AI-generated documents, spreadsheets, and slide decks across core workflows.
• Ensure accuracy and regulatory alignment of reports, dossiers, and publications.

Skills

CSR authoring

Protocol synopses

Regulatory dossiers

ICH-GCP knowledge

Job description

Ethos is partnering with a leading AI-focused lab to engage experienced clinical research associates. You will author, review, and refine AI-assisted clinical documents, including study reports and regulatory materials, maintaining high scientific rigor.

Applicants should have 5+ years in clinical research or regulatory affairs and deliver precise, well-structured documents for flexible, remote, part-time work at.$100/hour, ASAP 시작.