Scientific Writer

You will be responsible for the following key tasks: - Develop, write, and edit various scientific manuscripts, review articles, case studies, and conference abstracts/posters. - Prepare regulatory and clinical documents such as clinical study reports, investigator brochures, patient information leaflets, and regulatory dossiers. - Create medical communication materials including slide decks, CME content, and white papers tailored for healthcare professionals. - Collaborate effectively with researchers, clinicians, and regulatory teams to ensure accuracy, consistency, and compliance with journal/regulatory requirements. - Conduct thorough literature reviews and ensure precise referencing using platforms like PubMed and Scopus. - Ensure that all documents adhere to ICMJE, GCP, CONSORT, and other journal-specific guidelines. - Maintain exceptionally high standards of clarity, accuracy, and scientific integrity. Your qualifications and skills should include: - A Masters or PhD in Life Sciences, Pharmacy, Biotechnology, or Clinical Research. - At least 3 years of experience in scientific or medical writing; however, exceptional freshers with strong writing abilities may also be considered. - Proficient command of the English language, grammar, and scientific terminology. - Familiarity with journal submission processes and reference management software such as EndNote, Mendeley, and Zotero. - Knowledge of regulatory writing, including CSR and CTD/eCTD modules, would be a valuable asset. - Excellent communication skills, keen attention to detail, and the ability to consistently meet deadlines.,