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Medical Information And Adverse Event Intake Specialist With Dutch Language (12-Month Fixed Term...

0-2 years
Not Disclosed
10 June 3, 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

 

Job Title:

Medical Information and Adverse Event Intake Specialist (Dutch & English) – 12-Month Fixed Term Contract


Location:

Reading, United Kingdom (Remote/Hybrid/Office – Flexible)


Start Date:

June 2, 2025
Closing Date: July 2, 2025


Employer:

IQVIA
https://jobs.iqvia.com


About the Role:

This is a patient safety-focused position involving direct interaction with healthcare professionals and patients, supporting the collection and processing of adverse events (AEs) and medical information inquiries. This role plays a key part in pharmacovigilance and product quality surveillance and is critical to ensuring compliance and safeguarding public health.

This is a 12-month fixed term contract, with flexible work arrangements—remote, hybrid, or office-based in Reading.


Key Responsibilities:

  • Respond to medical inquiries and AE reports from HCPs and consumers via phone and email.

  • Process AE and product quality data, perform coding, data entry, and case tracking in Lifecycle Safety systems.

  • Maintain regulatory compliance and accuracy in documentation and case processing.

  • Collaborate with internal teams and contribute to quality improvement, training, and project updates.

  • Support project metrics reporting and client communications as required.


Required Qualifications & Skills:

  • Bachelor’s Degree in Life Sciences or related field.

  • Fluent Dutch (C2/native) and strong English (minimum C1) proficiency—both written and spoken.

  • Prior experience in pharmacovigilance, medical information, or safety case processing is an advantage.

  • Strong attention to detail and accuracy.

  • Proven ability to manage multiple priorities and work independently.

  • Excellent organizational, time management, and communication skills.


Why IQVIA?

  • Join a diverse global team driving innovation in healthcare.

  • Career development pathways, mentoring, and continuous training.

  • Work in a company that values diversity, inclusion, and authenticity.

  • Help improve patient outcomes and contribute to global health.


Important Note:

UK visa sponsorship is not available for this role.


Apply Now:

https://jobs.iqvia.com