MLR Technical Review specialist, Medical Communications

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When our values align, there's no limit to what we can achieve. At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do. Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference. Cross-check scientific information against cited references & ensure data accuracy and completeness Review/Add Anchor links to appropriate highlighted references (if capacity allows and for markets that already have Reference tagging) Reference QC: ensure reference integrity, propose update if appropriate, ensure statements are still aligned with latest data (e.g. update to latest KDIGO guide) Ensure alignment with latest approved product label (local) and flag any off-label communication. QC Essential Information like ISI, Brand & Generic Names, AE Reporting, etc. Review Footnote information, Terminology & Citation Style to ensure consistency through-out materials. Perform basic/high-level QC of asset - Branding, Style, Format, Grammar, Spelling and Punctuation Quality Check and/or create accurate documentation and checklists for Asset Technical and MLR Review/Creation Based on local guidelines, practices and regulations

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