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Medical Information And Adverse Event Intake Specialist With German And English Language

0-2 years
Not Disclosed
10 Feb. 4, 2025
Job Description
Job Type: Full Time Education: B.Pharm 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

Medical Information and Adverse Event Intake Specialist – Oeiras (medical-information-adverse-event-intake-oeiras)

Employer: IQVIA
Location: Oeiras
Start Date: 1 Feb 2025
Closing Date: 3 Mar 2025

Job Overview:

IQVIA, a global leader in pharmaceutical safety services, is seeking a Medical Information and Adverse Event Intake Specialist with expertise in German (C2/native) and English (C1) to join its growing team. This role involves handling medical information inquiries, adverse event reporting, and product quality complaints, ensuring the safety of pharmaceutical products worldwide.

Key Responsibilities:

  • Provide phone support to healthcare professionals and consumers regarding adverse events, medical inquiries, and product quality complaints (no commercial sales support).
  • Triage, review, assess, and process Lifecycle safety operational data, including data entry, medical coding, and narrative writing.
  • Document and manage incoming safety reports via telephone and email.
  • Collaborate with global teams, provide training, and mentor junior team members.
  • Communicate effectively with project teams and escalate potential issues proactively.
  • Participate in ongoing training and contribute to new safety initiatives.

Required Qualifications & Skills:

  • Bachelor’s Degree in Pharmacy (Mandatory).
  • Fluency in German (C2/native) and English (C1).
  • Strong attention to detail and accuracy in safety documentation.
  • Excellent organizational and time management skills.
  • Ability to manage multiple projects, prioritize tasks, and work independently.

Why Join IQVIA?

IQVIA is a global leader in clinical research, healthcare intelligence, and pharmaceutical innovation. We foster an inclusive culture where diverse perspectives drive smarter healthcare solutions. At IQVIA, you’ll have the opportunity to accelerate medical advancements and contribute to global health.

Apply now and be part of our mission to create a healthier world!