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The Safety Data Lead is responsible for the analysis and interpretation ofadverse experience (AE) reports of varying complexity in compliance with regulatory requirements and internal processes. Working under the supervision of a Manager in the Global Pharmacovigilance Case Management (GPVCM) the Safety Data Lead executes AE case management activities for both investigational and marketed products in accordance with specific therapeutic area standards. Collaboration with internal and external stakeholders is essential to maintain high quality and timely execution of the processes.
Among other tasks the Safety Data Lead is responsible for:
Education and other Qualifications:
Core Competencies:
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Employee Status:
RegularRelocation:
No relocationVISA Sponsorship:
NoTravel Requirements:
No Travel RequiredFlexible Work Arrangements:
HybridShift:
Not IndicatedValid Driving License:
NoHazardous Material(s):
N/ARequired Skills:
Adaptability Adaptability Business Business Acumen Case Management Clinical Data Cleaning Clinical Data Management Clinical Knowledge Customer-Focused Data Analysis Database Development Data Interpretations Data Processing Data Quality Assurance Data Review Data Science Data Validation Data Visualization Electronic Data Capture (EDC) Internal Processes Learning Agility Pharmaceutical Management Pharmacovigilance PL/SQL (Programming Language) Process Standardization 2 morePreferred Skills:
Job Posting End Date:
10/31/2025*A job posting is effective until 11:59:59PM on the day BEFOREthe listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.
Full-Time