MLR Technical Review specialist, Medical Communications

<p><b>When our values align, there&#39;s no limit to what we can achieve.</b><br /> <br />At Parexel, we all share the same goal - to improve the world&#39;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.</p><p>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&#39;re committed to making a difference.</p><p></p><p></p><ul><li>Cross-check scientific information against cited references &amp; ensure data accuracy and completeness</li><li>Review/Add Anchor links to appropriate highlighted references (if capacity allows and for markets that already have Reference tagging)</li><li>Reference QC: ensure reference integrity, propose update if appropriate, ensure statements are still aligned with latest data (e.g. update to latest KDIGO guide)</li><li>Ensure alignment with latest approved product label (local) and flag any off-label communication.</li><li>QC Essential Information like ISI, Brand &amp; Generic Names, AE Reporting, etc.</li><li>Review Footnote information, Terminology &amp; Citation Style to ensure consistency through-out materials.</li><li>Perform basic/high-level QC of asset - Branding, Style, Format, Grammar, Spelling and Punctuation</li><li>Quality Check and/or create accurate documentation and checklists for Asset Technical and MLR Review/Creation Based on local guidelines, practices and regulations</li></ul>