Scientist I
- Prioritize workload for US OTC/Medical Devices & Hospital visit cases, data entry, MedDRA coding, and case narrative completion into the Post-marketing Safety database.
- Reconcile daily cases received from Consumer Care Center, identify missing cases, and correct errors in the database.
- Provide feedback regarding database issues and communicate discrepancies to relevant teams.
- Support team projects related to case data completion and serve as a backup for statistical report preparation.
- Perform data extraction for global safety analyses and validate data accuracy.
- A completed BS or MS in biology or a related field with case processing and data exploitation experience in pharmacovigilance.
- Minimum of 3-5 years of relevant experience in safety data management or pharmacovigilance.
- Experience with MedDRA coding is preferred.
- Basic understanding of US regulations related to post-marketing safety is advantageous.
- Excellent verbal and written communication skills, with strong organizational abilities.
- Opportunity to work in a dynamic and innovative environment focused on safety and scientific excellence.
- Engage with a diverse team of talented professionals committed to advancing healthcare products.
- Gain valuable experience in global safety data management and regulatory compliance.
- Participate in ongoing training and professional development initiatives.
- Be part of a company dedicated to responsible and sustainable beauty and healthcare solutions.
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