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Adverse Event Intake Specialist With English Language

Iqvia

2+ years

Not Disclosed

Oeiras

10 March 26, 2025

Job Description

Job Type: Full Time Education: B.Sc./M.Sc./B.Pharm/M.Pharm/Life science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Adverse Event Intake Specialist with English Language - Oeiras (IQVIA)
Date: March 21, 2025
Location: Oeiras, Portugal
Company: IQVIA
Closing Date: March 25, 2025

Who we are:
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 that help improve patient outcomes and population health worldwide.

The opportunity:
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 ensure the safety profiles of products marketed around the world, with development opportunities to provide oversight on projects and teams.

Key Responsibilities:

Perform Pharmacovigilance activities per project requirements.
Collect and track incoming Adverse Events and endpoint information.
Receive, review, and interpret medical reports.
Process safety data according to applicable regulations, guidelines, Standard Operating Procedures (SOPs), and project requirements.
Determine initial/update status of incoming events.
Code Adverse Events and Products, write narratives, and perform literature-related activities within internal/project timelines.
Ensure quality, productivity, and delivery standards per project requirements.
Identify quality problems and escalate them to senior team members.
Attend project team meetings and provide feedback to the operations manager on any challenges/issues or successes.

Your experience and qualifications:
Requirements:

Education: Bachelor's Degree in Life Science or healthcare-related discipline.
Language: Excellent written and verbal skills in English (minimum C1 level).

Skills and Abilities:

Willingness and aptitude to learn new skills across Lifecycle Safety service lines.
Strong attention to detail and accuracy, maintaining consistently high-quality standards.
Excellent organizational and time management skills.
Ability to establish and maintain effective working relationships with coworkers, managers, and clients.
Capability to work effectively on multiple projects simultaneously, organize own workload, and 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 improve outcomes for patients. Forge a career with greater purpose, make an impact, and never stop learning.

Diversity and Inclusion Commitment:
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.

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Adverse Event Intake Specialist With English Language

Job Description

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