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