Supervisor, Pharmacovigilance
Clinical Careers Page(1 month ago)
About this role
A Pharmacovigilance Supervisor at ICON supports the oversight of drug safety activities within clinical development and marketed product programs, contributing to patient safety and regulatory adherence. The role is part of ICON’s global clinical research organization and is based in Brazil as a fully remote position.
Required Skills
- Pharmacovigilance
- Safety Reporting
- Regulatory Compliance
- Safety Data
- Data Analysis
- Team Leadership
- Training
- Communication
- Clinical Trials
- Detail Orientation
Qualifications
- Bachelor's Degree in Life Sciences or Pharmacy
About Clinical Careers Page
iconplc.comICON 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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