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

2+ years
Not Disclosed
10 Nov. 21, 2024
Job Description
Job Type: Full Time Remote Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences 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 with Hungarian and English

Company: IQVIA

Location: Home Based / Hybrid / Office-based (Flexible)

Job Overview:
IQVIA is looking for a Medical Information and Adverse Event Intake Specialist who will play a crucial role in Patient Safety. You will be the first point of contact for healthcare professionals (HCPs) and patients, processing safety and product quality information to help optimize the safety profiles of pharmaceutical products across various therapeutic areas. This is a highly visible and important role, ensuring that patient safety remains at the forefront of IQVIA’s operations.

Key Responsibilities:

  • HCP and Consumer Support: Provide phone support to healthcare professionals and consumers for adverse events, product quality complaints, medical inquiries, and product support. Note: This role does NOT include commercial sales support.
  • Data Management: Process Lifecycle safety operational data, track and enter information into safety databases, code medical terminology, and perform quality control to ensure data integrity.
  • Case Documentation: Receive and document incoming calls and emails related to safety data from investigative sites or other sources.
  • Team Collaboration: Build a positive team environment, provide training and mentoring for less experienced team members, and lead by example.
  • Project Liaison: Communicate with Project Managers, identifying issues, providing technical support, generating reports, and suggesting process improvements.
  • Training and Process Improvements: Participate in training sessions, working groups, and contribute to the identification and implementation of process efficiencies.

Minimum Required Education and Experience:

  • Education: Bachelor's Degree in a Life Science.
  • Language Skills: Proficiency in English (min. C1) and Hungarian (min. C2/native).
  • Experience: Previous experience in Lifecycle safety (e.g., Pharmacovigilance, CEVA, Medical Information, Safety Publishing, Risk Management) is an asset.
  • Skills:
    • Exceptional attention to detail and accuracy.
    • Strong organizational and time management skills to manage multiple projects and competing priorities.
    • Excellent verbal and written communication skills.

About IQVIA:

IQVIA is a global leader in clinical research services, healthcare intelligence, and commercial insights. Our mission is to connect people and ideas to accelerate the development and commercialization of medical treatments that improve patient outcomes worldwide.

For more information, visit IQVIA Careers.