Collection and processing of adverse event reports
Timely and accurate data entry
Preparation and submission of safety reports
You will contribute to pharmacovigilance and drug safety activities, taking responsibility for your deliverables and working collaboratively
Job Summary
You will contribute to pharmacovigilance and drug safety activities, taking responsibility for your deliverables and working collaboratively.
ICON plc is a world-leading healthcare intelligence and clinical research organization.
Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.
Matching Summary
You will contribute to pharmacovigilance and drug safety activities, taking responsibility for your deliverables and working collaboratively.
Skills & Requirements
Must-have
collection and processing of adverse event reports
timely and accurate data entry
preparation and submission of safety reports
collaboration with cross-functional teams
maintaining detailed records and documentation
Nice-to-have
fostering an inclusive environment
driving innovation and excellence
nurturing talent
Key Requirements
Bachelor's degree in life sciences, pharmacy, or related field
Basic understanding of pharmacovigilance principles
Relevant pharmacovigilance and drug safety experience
Strong attention to detail and organizational skills