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A leading company in the biotechnology sector is seeking a skilled medical/scientific writer. This role involves preparing clinical study reports and collaborating closely with various teams to ensure compliance and accuracy. Candidates should possess relevant degrees and experience within the pharmaceutical or healthcare industries.
Roles and Responsibilities;
Prepare clinical study reports (CSRs), investigator brochures, protocols, informed consent forms, and abstracts.
Write and edit scientific manuscripts, whitepapers, conference posters, slide decks, and product monographs.
Collaborate with medical affairs, clinical teams, and regulatory affairs to gather and verify scientific content.
Conduct literature reviews and stay updated on therapeutic areas and publication trends.
Ensure compliance with ICMJE, CONSORT, GPP3, and company writing guidelines.
Manage timelines, version control, and review workflows for assigned deliverables.
M.Sc / M.Pharm / PharmD / MBBS / BDS / Ph.D. in Life Sciences, Pharmacy, or Medicine.
Experience in medical/scientific writing in pharma, CRO, or healthcare publishing.
Familiarity with clinical trial data, ICH-GCP, and regulatory document structure.
Interested to apply can share you CV in Whatsapp/Call to9342735755