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