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1.0 - 6.0 years

0 - 0 Lacs

hyderabad, bangalore, united arab emirates

On-site

Roles and Responsibilities; Develop and review scientific content for clinical/scientific presentations, brochures, product monographs, patient education materials, slide decks, and white papers. Translate complex medical/scientific data into clear, engaging, and compliant communication for various audiences. Assist in the creation of publication plans, scientific abstracts, peer-reviewed articles, and regulatory documents. Collaborate with cross-functional teams including medical affairs, regulatory, pharmacovigilance, marketing, and clinical research. Ensure all content complies with company SOPs, regulatory standards, and industry codes. Conduct literature reviews, gap analysis, and content referencing from PubMed, Embase, Medline, etc. Attend medical conferences, KOL discussions, and advisory boards for content development and insight gathering. Qualifications & Experience: B.Pharm / M.Pharm / PharmD / MBBS / BDS / BAMS / MSc (Life Sciences, Biotechnology, Microbiology) Certification or diploma in medical writing or scientific communication (preferred) Interested to apply can share you CV in Whatsapp/Call to 9342735755

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