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 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.