La siguiente información tiene como objetivo proporcionar a los posibles candidatos una mejor comprensión de los requisitos para este puesto.
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 integral 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 metrics 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
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