Pharmacovigilance Specialist
hace 6 días
Job Overview
As a Pharmacovigilance Specialist at IQVIA, you will play a critical role in ensuring the safety and efficacy of pharmaceutical products in clinical trials. Under moderate supervision, you will 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 Research Sites and Units (RSU).
- Submit safety reports (periodic and expedited) in a timely manner.
- Submit Serious Adverse Events (SAE) and Suspected Unexpected Serious Adverse Reactions (SUSAR) to the Regulatory Authority (RA) on time, in accordance with 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, such as ensuring compliance with regulatory requirements and updating relevant documentation.
Requirements
To be successful in this role, you will need:
- A Bachelor's Degree in Life Sciences or a related field.
- 1-2 years of experience in pharmacovigilance, preferably in clinical studies.
- Fluency in conversational English.
At IQVIA, we are committed to pushing the boundaries of human science and data science to make a meaningful impact on the life sciences industry. If you are passionate about ensuring the safety and efficacy of pharmaceutical products, we encourage you to apply for this exciting opportunity.
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