Pharmacovigilance Specialist
hace 4 semanas
Job Overview
At IQVIA, we are seeking a skilled Pharmacovigilance Specialist to execute feasibility, site identification, regulatory, start-up, and maintenance activities in accordance with regulations, SOPs, and project requirements at the regional or country level.
Key Responsibilities
- Execute pharmacovigilance processes applicable to RSU.
- Submit safety reports (periodic and expedited) in a timely manner.
- Ensure submission of SAE/SUSAR to RA on time for applicable studies according to regulatory timelines.
- Perform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements, and contractual/budgetary guidelines.
- May also include maintenance activities.
Requirements
- Bachelor's Degree in Life Sciences or a related field.
- 1-2 years of pharmacovigilance experience in clinical studies.
- Fluent conversational English.
IQVIA is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world.
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