Pharmacovigilance Supervisor

Clinical Careers Page(1 day ago)

Sao Paulo, BrazilOnsiteFull TimeMedior$64,174 - $87,772 (estimated)Pharmacovigilance

About this role

ICON plc is seeking a Pharmacovigilance Supervisor to oversee safety monitoring and reporting of adverse events in clinical trials and marketed products. The role involves managing pharmacovigilance activities, ensuring compliance with regulations, and leading a team to maintain high standards of patient safety.

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Required Skills

Pharmacovigilance
Safety Monitoring
Regulatory Compliance
Team Leadership
Data Analysis
Clinical Trials
Drug Safety
SOPs
Reporting
Medical Writing

Qualifications

Bachelor’s degree in life sciences, pharmacy, or related field

About Clinical Careers Page

iconplc.com

ICON plc is a global clinical research organisation (CRO) that provides outsourced clinical development and commercialisation services to pharmaceutical, biotechnology and medical device companies. It offers end-to-end drug and device development support — including clinical trial management across phases, data management and biostatistics, regulatory and safety/pharmacovigilance, and commercialisation and market-access services. ICON combines scientific and therapeutic expertise with technology and a scalable global operations network to accelerate development and bring therapies to patients. Clients engage ICON for integrated, experienced CRO support across the full product lifecycle.

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