<p><b>Responsibilities:</b></p><ul><li>Cross-check scientific information against cited references and ensure accuracy (fact checking)</li><li>Ensure consistency with approved product labelling and check for any off-label communication</li><li>Ensure translation accuracy for localized material (against global version) and adherence to approved local label (indications, disease state description, population etc. per local label)</li><li>Cross check consistency in reference citation style</li><li>Verify presence of essential information like brand and generic names, AE reporting, presence of API etc, (based on checklist)</li><li>Reference link and annotate assets in Veeva</li><li>Liaise with content development team stakeholders and provide clarification on content or references.</li><li>Ensure quality of review and submission of the jobs within the agreed-upon time frame.</li><li>Keep themselves updated on different products & TAs</li><li>Provide inputs on metrices such as SLAs, KPIs and other periodic reports.</li></ul><p><br></p><p><b>Requirements:</b></p><ul><li>Advanced bioscience or pharmacy/medical qualification.</li><li>Excellent communication ability, both verbal and written (both, Spanish and English), at all levels</li><li>Experience in pharmaceutical industry within medical affairs; experience working as a QC reviewer for promotional and non-promotional materials of prescription only medications.</li><li>Strong scientific acumen and ability to grasp complex therapeutic areas.</li><li>Good understanding of Global and Local regulations on advertising, promotion and scientific exchange.</li><li>Good multitasking, project management, team management and organizational skills.</li><li>Total experience – 2-4 years of pharmaceutical industry experience which includes medical affairs/medical information related content writing, review, literature reviews, publications support etc with 2-3 years of experience in promotional/non-promotional medical review.</li></ul><p></p>