Pharmacovigilance Regulatory Reporting

hace 19 horas


Ciudad de México IQVIA A tiempo completo

**Job Overview**- As a Regulatory Reporting Specialist, you will be involved in submitting safety reports to regulatory authorities. _Review, assess, and process safety data and information received from various sources. Distribute reports/data to internal and external third parties following applicable regulations, Standard Operating Procedures (SOPs), and internal guidelines under the guidance and support of senior operation team members.**Essential Functions**- Process safety data according to applicable regulations, guidelines, SOPs, and project requirements.- Ensure compliance with quality, productivity, and delivery standards per project requirements.- Track cases as applicable to the project plan.- Identify and report quality problems to senior team members.- Liaise with different functional team members and health care professionals to address project-related issues.- Attend project team meetings and provide feedback to the operations manager on challenges, issues, or successes.**Qualifications**- Bachelor's degree in life sciences- Languages: Advanced level of **English**- **2-**3**years of experience in pharmacovigilance activities (mandatory) Specifically in regulatory reporting, will be highly valued.- Good knowledge of medical terminology and applicable safety databases.- Strong organizational skills, attention to detail, and ability to work independently and as part of a team.Work modality:100% home-basedCould be located in any Mexico city.



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