Spécialiste Principal (e), Pharmacovigilance / Senior Specialist, Pharmacovigilance
Imsapharma Com Ar
Hybrid
Adverse event management
Health authority submissions
Compliance monitoring
The Senior Specialist, Pharmacovigilance is responsible for adverse event management including aggregate and Individual Case Safety Report (ICSR) health authority submissions and compliance monitoring
Job Summary
The Senior Specialist, Pharmacovigilance is responsible for adverse event management including aggregate and Individual Case Safety Report (ICSR) health authority submissions and compliance monitoring.
They are also responsible for pharmacovigilance activities which may include but are not limited to: pharmacovigilance intake, management and negotiation of local pharmacovigilance agreements, and local due diligence activities.
The company embraces the value of bringing diverse, talented, and committed people together and is committed to fostering an inclusive and diverse workplace.
Matching Summary
The Senior Specialist, Pharmacovigilance is responsible for adverse event management including aggregate and Individual Case Safety Report (ICSR) health authority submissions and compliance monitoring.
Skills & Requirements
Must-have
Adverse Event Management
Health Authority Submissions
Compliance Monitoring
Pharmacovigilance Regulations
Local Pharmacovigilance Agreements
Nice-to-have
Strategic Thinking
Cross-functional Collaboration
Talent Development
Process Improvement Initiatives
Key Requirements
Minimum 5 years pharmaceutical industry experience
Bachelor degree in Health, life science, nursing, medical science degree or equivalent