Medical Writer

Role & responsibilities

An entry-level Medical Writer to prepare accurate, well-researched scientific and regulatory documents for clinical and healthcare audiences.

Key Responsibilities

Draft or support clinical study reports, protocols and manuscripts

Conduct literature review and summarise scientific/clinical data

Support preparation of regulatory writing documents (CTD modules, dossiers)

Ensure content is accurate, consistent and follows journal/regulatory guidelines

Collaborate with clinical, regulatory and research teams for content inputs

Proofread and edit documents for scientific accuracy and clarity

Stay updated with GCP, ICH guidelines and referencing standards (AMA/Vancouver style)

Preferred candidate profile

Basic knowledge of MS Office (Word, Excel, PowerPoint)

Good written and verbal communication skills

Attention to detail and documentation discipline

Willingness to learn and work in a regulated, compliance-driven environment

Strong command over English grammar and scientific writing style