Adverse Event Intake Specialist with Dutch and English language
Apply your knowledge and expertise, including complex decision making, to review, assess, and process safety and product quality information. Be a part of a global team to help ensure the safety profiles of products marketed around the world, with development opportunities to ultimately provide oversight on projects and teams.
Summary:
Review, assess, and process safety data and information across service lines, received from various sources, and distribute reports to both internal and external third parties, following applicable regulations, SOPs, and internal guidelines under the guidance and support of senior operation team members.
Key responsibilities:
- Perform pharmacovigilance activities per project requirements.
- Collect and track incoming adverse events and endpoint information.
- Review and interpret medical reports.
- Process safety data according to applicable regulations, guidelines, SOPs, and project requirements.
- Determine the initial/update status of incoming events.
- Code adverse events and products, write narratives, and perform
- related activities as per internal/project timelines. - Ensure to meet quality, productivity, and delivery standards per project requirements.
- Identify quality problems and escalate to senior team members.
- Participate in project team meetings and provide feedback to the operations manager on challenges, issues, or successes.
Minimum Required Education and Experience:
- Bachelor’s Degree in Life Sciences or a
- related discipline is required. - Excellent written and verbal skills in English (min. C1) and Dutch (min. C2 or native).
Skills and Abilities:
- Willingness and aptitude to learn new skills across our Lifecycle Safety service lines.
- Excellent attention to detail and accuracy, maintaining
- quality standards. - Strong organizational 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 and manage priorities.
Join Us
Making a positive impact on human health requires insight, curiosity, and intellectual courage. It takes brave minds pushing boundaries to transform healthcare. Regardless of your role, you will have the opportunity to help our clients advance healthcare and improve patient outcomes. Forge a career with purpose, make an impact, and never stop learning.
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 medical treatments to improve patient outcomes and population health worldwide. Learn more at https://jobs. iqvia.com.
At IQVIA, we believe that diversity, inclusion, and belonging empower our mission to innovate for a healthier world. We value diverse perspectives and provide opportunities for all talented employees to contribute to smarter healthcare. When our employees bring their authentic selves, we achieve extraordinary results. Diverse teams foster innovation and collaboration, leading to better outcomes.
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Empresa: IQVIA Argentina Localização: Oeiras
Oeiras, Distrito de Lisboa, PortugalPublicado: 27. 6. 2025
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