IQVIA Inc is seeking a Farmacovigilance Scientist to lead safety aggregate reporting and analytics related to pharmacovigilance. The ideal candidate will possess a Bachelor's degree in a scientific or healthcare discipline, along with 2-4 years of relevant experience in safety reporting and regulatory compliance
Job Summary
Serve as principal owner of SARA deliverables, ensuring compliance with SLAs.
Lead, author, and finalize aggregate reports, conduct literature surveillance, and manage safety signals.
Interface with clients and internal functional groups, participate in audits, and contribute to departmental goals.
Matching Summary
Match Score: 85
IQVIA Inc is seeking a Farmacovigilance Scientist to lead safety aggregate reporting and analytics related to pharmacovigilance. The ideal candidate will possess a Bachelor's degree in a scientific or healthcare discipline, along with 2-4 years of relevant experience in safety reporting and regulatory compliance.
Skills & Requirements
Must-have
Aggregate report authoring
Literature safety surveillance
Signal detection and evaluation
Regulatory agency responses
Client and functional group interface
Nice-to-have
Mentorship and training
Technology and innovation contribution
Adaptability to changing demands
Independent thinking and decision making
Key Requirements
Bachelor's Degree in Scientific or Healthcare discipline
2-4 years relevant work experience
Knowledge of applicable global regulatory requirements (GCP, GVP, ICH)