Medical Writer / Scientific Writer

Location: Bengaluru / Hyderabad (India)

Employment Type: Full-time

Role summary

We are seeking highly skilled Medical Writers / Scientific Writers to join our team and contribute to the development of high-quality scientific and regulatory documents. The ideal candidate will have strong expertise in scientific communication, medical writing, and regulatory documentation, with the ability to translate complex data into clear, accurate, and compliant content.

Key Responsibilities

•Develop, write, and edit clinical, regulatory, and scientific documents (protocols, clinical study reports, manuscripts, abstracts, regulatory submissions, slide decks, white papers, etc.)
•Ensure documents comply with regulatory guidelines (ICH, GCP, FDA, EMA) and internal quality standards
•Perform literature searches and scientific reviews to support writing assignments
•Collaborate with clinical, medical, and regulatory teams to gather and validate data
•Translate complex medical/scientific information into clear, concise, and audience-appropriate content
•Maintain version control and document consistency across submissions and publications
•For senior writers: mentor junior writers and ensure quality review of deliverables

Skills & Qualifications

•Advanced degree in Life Sciences / Pharmacy / Medicine (M.Sc., M.Pharm, PhD, MBBS preferred)
•Strong knowledge of clinical research, drug development, and regulatory writing standards
•Excellent written and verbal communication skills with attention to detail
•Proficiency in Microsoft Office Suite and reference management tools
•Familiarity with publication guidelines (ICMJE, CONSORT, GPP) is a plus
•Ability to work independently and as part of cross-functional teams
•Strong analytical, research, and project management skills

Experience

Medical Writer: 2–5 years of relevant experience in medical or scientific writing

Senior / Scientific Writer: 6–10 years with proven expertise in regulatory or publication writing