Consultant – Pharmacovigilance Pharmacist
Ividata Life Sciences
Posted: 10/21/2026Consulting Pharmacist – Quality and Pharmacovigilance
Ividata Life Sciences
Posted: 9/25/2026Consultant – Pharmacovigilance Pharmacist
Ividata Life SciencesCore Competencies
Role fitCore Competencies
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Demonstrates strong expertise in pharmacovigilance case management, including proficiency with safety databases and the MedDRA dictionary. Capable of coordinating communication across teams and preparing detailed reports while adhering to regulatory requirements.
Highest-signal resume keywords
Pharmacovigilance Case ManagementSafety Database ProficiencyMedDRA Dictionary KnowledgeRegulatory Environment KnowledgeBachelor’s to Master’s Degree in Pharmacovigilance
About the role
Key responsibilities & impact- Collect, document, and follow up on pharmacovigilance notifications and cases from various sources
- Enter, document, and monitor cases in pharmacovigilance databases in compliance with timelines and quality requirements
- Anonymize documents, perform quality checks, and review the medical consistency of case files before their transfer to central databases
- Monitor indicators and reporting tools related to pharmacovigilance activities
- Coordinate communication with local and global teams, as well as external partners involved in safety data management
- Contribute to the review of local pharmacovigilance procedures, signal detection, and the preparation of periodic reports
- Participate in scientific and regulatory monitoring and literature management related to pharmacovigilance
- Contribute to the preparation of reports and summaries for stakeholders and management
- Work on high-value projects in collaboration with an international pharmaceutical industry client
Requirements
What you’ll need- Bachelor’s to Master’s degree in pharmacovigilance, clinical drug development, or an equivalent field
- A pharmacy degree is preferred
- At least 5 years of experience in pharmacovigilance case management within the pharmaceutical industry, a pharmaceutical company, or a CRO
- Strong expertise in pharmacovigilance case management
- Proficiency with safety databases; experience with ARGUS is highly desirable
- Proficiency with the MedDRA dictionary
- Good knowledge of the pharmacovigilance regulatory environment
- Knowledge of case management processes for cases received from various sources
- Highly organized, detail-oriented, and able to prioritize; autonomous, analytical, and capable of producing reports; a strong team player with excellent adaptability
- Professional and fluent English, both written and spoken
Benefits
Comp & perks- Remote work opportunities as part of a hybrid role
- A stimulating, collaborative, and constantly evolving environment
- High-impact assignments at the forefront of healthcare innovation
- Collaboration with passionate experts and leading industry players
- The opportunity to develop expertise across the full product life cycle
ATS Keywords
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Hard Skills
Pharmacovigilance Case ManagementSafety Database ProficiencyMedDRA Dictionary KnowledgeQuality ChecksSignal DetectionReport PreparationCase Management ProcessesScientific MonitoringRegulatory MonitoringData Anonymization
Soft Skills
Highly OrganizedDetail-OrientedAnalyticalStrong Team PlayerExcellent Adaptability
Tools & Technologies
ARGUSPharmacovigilance Databases
Industry Keywords
Pharmaceutical IndustryClinical Drug DevelopmentPharmacovigilance ProceduresSafety Data ManagementCRO