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We are seeking a Pharmacovigilance Analyst to join our team on a contract basis to cover maternity leave. This role will be temporary, with the contract lasting until the end of 2026.

Role Purpose:

Provides support across the business on pharmacovigilance within the PMR space. Ensures GVP Module VI compliance on specific projects and working with specific clients. Maintains internal PV training. Conducts data entry of safety cases in client systems and forms.

Principal Accountabilities:

Analyses Primary Market Research questionnaires and client product labels to identify reportable safety data in projects of lower complexity.

Programs basic logic filters in internal IQVIA systems to monitor and report safety data.

Ensures accurate data entry of safety information in client systems and reporting forms.

Ensures PV compliance with client requirements including training, reporting and reconciliation.

Responds to client queries, follow-up requests and customer complaints (internal and external).

Minimum Education, Experience, & Specialized Knowledge required:

Bachelor’s degree or equivalent. Working knowledge of pharmacovigilance requirements and processes.

Excellent command of English is essential.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com