About Clinforge Clinforge Clinical Research Solutions Pvt. Ltd. is a growing Contract Research Organization (CRO) dedicated to delivering high-quality services in clinical research, regulatory affairs, pharmacovigilance, and scientific/medical writing . Our mission is to bridge science and communication by transforming complex research into impactful knowledge. Key Responsibilities Develop, write, and edit scientific manuscripts, review articles, case studies, and conference abstracts/posters . Prepare regulatory and clinical documents (clinical study reports, investigator brochures, patient information leaflets, regulatory dossiers). Create medical communication materials including slide decks, CME content, and white papers for healthcare professionals. Collaborate with researchers, clinicians, and regulatory teams to ensure accuracy, consistency, and compliance with journal/regulatory requirements. Conduct literature reviews and ensure referencing accuracy (PubMed, Scopus, etc.). Ensure documents follow ICMJE, GCP, CONSORT, and journal-specific guidelines . Maintain high standards of clarity, accuracy, and scientific integrity . Qualifications & Skills Master’s or PhD in Life Sciences / Pharmacy / Biotechnology / Clinical Research . 1–3 years of experience in scientific or medical writing (Fresher with strong writing skills may be considered). Strong command of English language, grammar, and scientific terminology . Familiarity with journal submission processes and reference management software (EndNote, Mendeley, Zotero). Knowledge of regulatory writing (CSR, CTD/eCTD modules) will be an added advantage. Excellent communication, attention to detail, and ability to meet deadlines.
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.,