Review, assess, and process safety data and information from various sources. Distribute reports/data to internal and external third parties following applicable regulations, Standard Operating Procedures (SOPs), and internal guidelines with support from senior team members.

Essential Functions

• Prioritize and complete assigned training on time.

• Process safety data according to regulations, guidelines, SOPs, and project requirements.

• Perform pharmacovigilance activities, including collecting and tracking adverse events (AEs), determining event status, database entry, coding AEs and products, writing narratives, and literature-related activities.

• Ensure quality and productivity standards are met per project requirements.

• Maintain compliance with all project-related processes and activities.

• Identify and report quality problems to senior team members.

• Liaise with project management, clinical, data management teams, and healthcare professionals to address project-related issues.

Qualifications

• Bachelor's degree in life sciences or related field required.

• Up to 3 years of relevant experience, including up to 1 year of pharmacovigilance experience, highly valued.

• Proficiency in English is a must.

• Good knowledge of medical terminology and applicable safety databases.

• Strong organizational, time management, and communication skills.

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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