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Medical Information and Adverse Event Specialist
hace 2 meses
Job Summary
IQVIA LLC is seeking a highly skilled Medical Information and Adverse Event Specialist to join our team. As a key member of our Pharmacovigilance team, you will play a critical role in ensuring the safety of patients by providing medical information and processing adverse event reports.
Key Responsibilities
- Provide medical information and support to healthcare professionals and patients regarding adverse events, product quality complaints, and medical inquiries.
- Process and analyze safety operational data, perform data entry, and generate queries pertinent to the case.
- Collaborate with the Lifecycle Safety team to build a positive and collaborative team environment.
- Provide regular feedback to operations team managers on project metrics and challenges.
- Liaise with Project Managers to identify issues and propose solutions.
Requirements
- Bachelor's Degree in a Life Science.
- Excellent written and verbal skills in English and Danish.
- Experience in Pharmacovigilance or a related field is an asset.
- Excellent attention to detail and accuracy maintaining consistently high-quality standards.
- Ability to work effectively on multiple projects simultaneously.
About IQVIA LLC
IQVIA LLC 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.
