Scientific Writer

You will be responsible for the following key tasks: - Developing, writing, and editing scientific manuscripts, review articles, case studies, and conference abstracts/posters. - Preparing regulatory and clinical documents such as clinical study reports, investigator brochures, patient information leaflets, and regulatory dossiers. - Creating medical communication materials like slide decks, CME content, and white papers tailored for healthcare professionals. - Collaborating with researchers, clinicians, and regulatory teams to ensure accuracy, consistency, and compliance with journal/regulatory requirements. - Conducting literature reviews and ensuring referencing accuracy using platforms like PubMed, Scopus, etc. - Ensuring all documents adhere to ICMJE, GCP, CONSORT, and journal-specific guidelines. - Maintaining high standards of clarity, accuracy, and scientific integrity. You should possess the following qualifications and skills: - Masters or PhD in Life Sciences, Pharmacy, Biotechnology, or Clinical Research. - Minimum of 3 years of experience in scientific or medical writing (Freshers with strong writing skills may be considered). - Strong command over the English language, grammar, and scientific terminology. - Familiarity with journal submission processes and reference management software like EndNote, Mendeley, or Zotero. - Knowledge of regulatory writing including CSR, CTD/eCTD modules will be an added advantage. - Excellent communication skills, attention to detail, and ability to meet deadlines. You will be responsible for the following key tasks: - Developing, writing, and editing scientific manuscripts, review articles, case studies, and conference abstracts/posters. - Preparing regulatory and clinical documents such as clinical study reports, investigator brochures, patient information leaflets, and regulatory dossiers. - Creating medical communication materials like slide decks, CME content, and white papers tailored for healthcare professionals. - Collaborating with researchers, clinicians, and regulatory teams to ensure accuracy, consistency, and compliance with journal/regulatory requirements. - Conducting literature reviews and ensuring referencing accuracy using platforms like PubMed, Scopus, etc. - Ensuring all documents adhere to ICMJE, GCP, CONSORT, and journal-specific guidelines. - Maintaining high standards of clarity, accuracy, and scientific integrity. You should possess the following qualifications and skills: - Masters or PhD in Life Sciences, Pharmacy, Biotechnology, or Clinical Research. - Minimum of 3 years of experience in scientific or medical writing (Freshers with strong writing skills may be considered). - Strong command over the English language, grammar, and scientific terminology. - Familiarity with journal submission processes and reference management software like EndNote, Mendeley, or Zotero. - Knowledge of regulatory writing including CSR, CTD/eCTD modules will be an added advantage. - Excellent communication skills, attention to detail, and ability to meet deadlines.