MLR Technical Review specialist, Medical Communications
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Job Location:
Monthly Salary:
Posted on:
Yesterday
Vacancies:
1 Vacancy
Job Summary
When our values align theres no limit to what we can achieve.
At Parexel we all share the same goal - to improve the worlds 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 were 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
Required Experience:
IC
Key Skills
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- hardware
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- Technical Support
- Software Applications
About Company
Parexel is in the business of improving the world’s health. We do this by providing a suite of biopharmaceutical services that help clients across the globe transform scientific discoveries into new treatments. From clinical trials to regulatory, consulting, and market access, our the ... View more
