Remote Medical Writer: Scientific & Regulatory Documents

MNC JOBS INFO; Singapore; Hybrid; SGD 90,000 - 130,000; Full time

Benefits offered by this job

Remote or hybrid working options

Professional development opportunities

Competitive compensation

Insurance and employment entitlements

Job summary

MNC JOBS INFO is seeking a detail-oriented Medical Writer – Scientific and Regulatory Documents to produce and maintain high-quality clinical and regulatory documentation for healthcare professionals, researchers, and authorities.

The role involves translating complex clinical data into clear, accurate content, ensuring regulatory compliance, and collaborating with clinical teams, statisticians, and QA across the study lifecycle.

Qualifications

• Bachelor’s degree or higher in Life Sciences or related field.
• Masters/PharmD/PhD may be preferred for certain positions.
• Certification/training in medical writing or regulatory affairs is valuable.
• Understanding of ICH‑GCP and clinical documentation is desirable.

Responsibilities

• Prepare, draft, review, and edit scientific, medical, and regulatory documents.
• Develop protocols, reports, brochures, informed consent forms, and regulatory submissions.
• Write scientific summaries and literature reviews with evidence-based content.
• Ensure accuracy and consistency with data, sources, and templates.
• Maintain version control and document traceability throughout studies.

Skills

Excellent written English

Scientific terminology

Document structuring/editing

Templates and style guides

Reference management

Reviewer feedback incorporation

Education

Bachelor's degree in Life Sciences or related

Master's degree / PharmD / PhD preferred

Medical writing/regulatory training advantageous

ICH‑GCP familiarity desirable

Tools

Microsoft Word

Excel

PowerPoint

EndNote / Zotero / Mendeley

Job description

MNC JOBS INFO is seeking a detail-oriented Medical Writer – Scientific and Regulatory Documents to produce and maintain high-quality clinical and regulatory documentation for healthcare professionals, researchers, and authorities.

The role involves translating complex clinical data into clear, accurate content, ensuring regulatory compliance, and collaborating with clinical teams, statisticians, and QA across the study lifecycle.