Pharmacovigilance Specialist
hace 4 días
Job Overview
As a Pharmacovigilance Specialist at IQVIA, you will play a critical role in ensuring the safety of patients by executing 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
- Manage pharmacovigilance processes applicable to Research Sites and Units (RSU).
- Submit safety reports (periodic and expedited) in a timely manner.
- Collaborate with Regulatory Affairs to submit SAE/SUSAR reports on time, adhering to regulatory timelines.
- Perform site activation tasks at a country level, aligning with local and international regulations, SOPs, project requirements, and contractual guidelines.
- May also be responsible for 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 strive to push the boundaries of human science and data science to create a healthier world.
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