Role & responsibilities

- Draft, review, and edit scientific manuscripts, review articles, abstracts, and posters for publication in peer-reviewed journals.

- Ensure all scientific content complies with Good Publication Practices (GPP) and journal-specific editorial guidelines.

- Collaborate with cross-functional R&D; and clinical teams to interpret experimental findings and clinical datasets.

- Conduct in-depth Systematic Literature Reviews (SLR) using recognized scientific databases (PubMed, Scopus, Web of Science).

- Prepare and format vital regulatory documents, including Clinical Study Reports (CSR) and study protocols.

- Support the drafting of technical reports, white papers, and patent/IP documentation (invention disclosures).

- Manage the end-to-end publication process, utilizing reference management tools and content management systems.





- Perform rigorous quality control checks for scientific accuracy, formatting, and data integrity.

Preferred candidate profile

- Masters degree in Pharmacy (M.Pharm), Life Sciences, Biotechnology, Biology, or a related discipline.

- Strong foundational knowledge in scientific writing, manuscript preparation, or medical communications (published papers are a strong advantage).

- Familiarity with clinical research processes, therapeutic areas, and regulatory documentation.

- Excellent command of the English language with a proven ability to translate complex data into transparent, concise narratives.

- Proficiency in utilizing scientific literature databases and reference management software.

📌 Scientific Writer (Bengaluru)
🏢 Airvin Skills
📍 Bengaluru