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Adverse Event Specialist with English Language Support
1 tydzień temu
We are looking for a highly motivated Safety Data Analyst to join our team at IQVIA. As an Adverse Event Intake Specialist with English language support, you will be responsible for reviewing, assessing, and processing safety and product quality information.
Your key responsibilities will include:
- Performing Pharmacovigilance activities per project requirement.
- Collecting and tracking incoming Adverse Events and endpoint information.
- Receiving, reviewing, and interpreting medical reports.
- Processing safety data according to applicable regulations, guidelines, Standard Operating procedures (SOPs), and project requirements.
- Determining initial/update status of incoming events.
- Coding Adverse Events and Products, writing narratives, and performing Literature related activities as per internal/project timelines.
- Ensuring meeting quality, productivity, and delivery standards per project requirements.
- Identifying quality problems, if any, and bringing them to the attention of senior team members.
- Attending project team meetings and providing feedback to operations manager on any challenges/issues or successes.
Skills and Abilities:
- Bachelor's Degree in Life Science or healthcare-related discipline is required.
- Excellent written and verbal skills in English (min. C1).
- Willingness and aptitude to learn new skills across our Lifecycle Safety service lines.
- Excellent attention to detail and accuracy maintaining consistently high-quality standards.
- Excellent organizational skills and time management skills.
- Ability to establish and maintain effective working relationships with coworkers, managers, and clients.
- Ability to work effectively on multiple projects simultaneously, organize own workload, and effectively manage competing priorities.
