Adverse Event Intake Specialist with Swedish 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 onwards to both internal and external third parties, following applicable regulations SOPs and internal guidelines under guidance and support of senior operation team members.

Key responsibilities:

• Performing Pharmacovigilance activities per project requirement.
• Collecting and tracking incoming Adverse Events and endpoint information.
• Receiving, reviewing and interpretation of 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.
• Ensure to meet quality, productivity, and delivery standards per project requirements.
• Identify quality problems, if any, and bring them to the attention of a senior team members.
• Attend project team meetings and provide feedback to operations manager on any challenges/issues or successes.

Minimum Required Education and Experience

• Bachelor's Degree in Life Science or healthcare related discipline is required
• Excellent written and verbal skills in English (min. C1) and Swedish (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 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.

Join Us
Making a positive impact on human health takes insight, curiosity, and intellectual courage. It takes brave minds, pushing the boundaries to transform healthcare. Regardless of your role, you will have the opportunity to play an important part in helping our clients drive healthcare forward and ultimately improve outcomes for patients. Forge a career with greater 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 innovative medical treatments to help 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 accelerate innovation for a healthier world. We create a culture of belonging by valuing the perspectives of all talented employees worldwide and providing them with the opportunity to power smarter healthcare for everyone, everywhere. When our talented employees bring their authentic selves and their diverse experiences to work, they enable us to accomplish extraordinary things. Multifaceted thought processes spark innovation. Multi-talented collaboration harnesses innovation to deliver superior outcomes.