Adverse Event Analyst
hace 2 días
We are seeking a highly organized and detail-oriented individual to join our team as an Adverse Event Analyst.
ResponsibilitiesThe successful candidate will be responsible for:
- Supporting the complaint handling unit.
- Assessing complaints for reportability to regulatory authorities.
- Executing based on the adverse event determination process.
- Preparing and submitting initial, supplemental, and final incident reports within regulatory timeframes.
- Bachelor's degree in biology, health sciences, engineering, or nursing preferred.
- 2+ years' experience in the medical device industry required.
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Adverse Event Manager
hace 6 días
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Management Trainee
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Medical Device Reporting Specialist
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Medical Device Surveillance Expert
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Safety Data Analyst
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Product Compliance Specialist
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Incident Management Coordinator
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Medical Surveillance Specialist
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Safety Data Management Specialist
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Regulatory Compliance Officer
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Business Intelligence Analyst T1
hace 6 días
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Medical Device Reporting Specialist
hace 6 días
San José, San José, Costa Rica Genpact A tiempo completoJob DescriptionGenpact is a global professional services and solutions firm delivering outcomes that shape the future. Our 125,000+ people across 30+ countries are driven by our innate curiosity, entrepreneurial agility, and desire to create lasting value for clients. Powered by our purpose – the relentless pursuit of a world that works better for people...
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Data Safety Management Lead
hace 1 día
San José, San José, Costa Rica Msd A tiempo completoJob DescriptionWe are seeking a highly skilled Senior Safety Data Specialist to join our team at Msd. As a member of our global pharmacovigilance organization, you will be responsible for ensuring the quality and integrity of our safety data.ResponsibilitiesProcess and analyze complex adverse event reports, identifying trends and patterns that inform...
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Global Pharmacovigilance Specialist
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hace 3 semanas
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