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Clinical Safety Associate
hace 2 semanas
As a Clinical Safety Associate, you will contribute to the delivery of high-quality clinical safety services at IQVIA. Your primary responsibilities will include reviewing and processing safety data, performing pharmacovigilance activities, and collaborating with cross-functional teams to address project-related issues.
**Responsibilities and Requirements**
- Prioritize and complete assigned training on time to stay current with regulations and guidelines.
- Process safety data according to applicable regulations, guidelines, and project requirements.
- Collect and track adverse events (AEs), determine event status, and perform database entry, coding AEs and products, writing narratives, and literature-related activities.
- Collaborate with project management, clinical, data management teams, and healthcare professionals to resolve project-related issues.
- 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.
- Excellent analytical and communication skills are necessary.
