Scientific Writer

Airvin Skills; Hyderabad, Chennai, Bengaluru; Hybrid; INR 300,000 - 700,000; Full time

Job summary

Airvin Skills in Hyderabad seeks a qualified professional to draft, review, and edit scientific manuscripts and abstracts for peer-reviewed journals. The role involves ensuring compliance with GPP and journal guidelines, and collaborating with cross-functional R&D and clinical teams to interpret data.

The candidate should have a strong background in scientific writing and experience with clinical research processes, regulatory documentation, and literature databases, with excellent English

Qualifications

• Strong foundation in scientific writing and manuscript preparation.
• Familiarity with clinical research processes and regulatory documentation.
• Ability to translate complex data into clear narratives in English.
• Experience using scientific databases and reference management tools.

Responsibilities

• Draft, review, and edit scientific manuscripts, review articles, abstracts, and posters for publication in peer-reviewed journals.
• Ensure all scientific content complies with GPP and journal guidelines.
• Collaborate with R&D and clinical teams to interpret experimental findings.
• Conduct Systematic Literature Reviews using PubMed, Scopus, Web of Science.
• Prepare regulatory documents including CSR and study protocols.
• Support drafting of technical reports, white papers, and patent/IP disclosures.
• Manage end-to-end publication process and perform quality control checks.

Skills

Scientific writing

Manuscript preparation

Medical communications

Data interpretation

Cross-functional collaboration

English language proficiency

Literature databases

Education

M.Pharm or Life Sciences or related discipline

Tools

Reference management software

Job description

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 clear, concise narratives.
• Proficiency in utilizing scientific literature databases and reference management software.