Responsibilities:
La siguiente información tiene como objetivo proporcionar a los posibles candidatos una mejor comprensión de los requisitos para este puesto.
* 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. xpzdshu
* 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.