Job Overview
Under moderate supervision, executes the feasibility, site identification regulatory, start-up, and maintenance activities in accordance with regulations, SOPs, and project requirements at the regional, or country level.

Essential Functions

• Pharmacovigilance processes applicable to RSU.
• Submission of safety reports (periodic and expedited)
• Submission of SAE/SUSAR to RA on time for the 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.

Qualifications

• Bachelor's Degree 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. Learn more at https://jobs.iqvia.com