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Medical Information Specialist With Latvian And English And Additional Foreign Language

2+ years
Not Disclosed
10 July 16, 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

 

Medical Information Specialist – Riga (Latvian & English + EU Language)

Location: Riga, Latvia (Remote/Hybrid/On-site)
Salary: Competitive
Employer: IQVIA
Start Date: 30 Jun 2025
Closing Date: 31 Jul 2025


Job Summary

IQVIA, a global leader in healthcare and clinical research, is hiring a Medical Information and Adverse Event Intake Specialist fluent in Latvian, English, and ideally German, French, or Italian. This is a pivotal patient safety role supporting global pharmacovigilance and product quality operations. Candidates can work remotely, in a hybrid setup, or from the Riga office.


Key Responsibilities

  • Deliver phone-based medical support to healthcare professionals and patients (excluding sales).

  • Document and process safety data, including product complaints and adverse events.

  • Input lifecycle safety data and code medical terminology accurately.

  • Perform quality checks, case closure, and coordinate translations.

  • Proactively communicate project updates, risks, and metrics to managers.

  • Provide peer mentorship and contribute to process improvement.

  • Support new initiative implementation and standard operating procedures.


Required Skills & Qualifications

  • Bachelor’s degree in Life Sciences or a related field.

  • Native-level fluency in Latvian and professional proficiency in English (C1 or higher).

  • Proficiency in an additional EU language (preferably German, French, or Italian).

  • Prior experience in pharmacovigilance, CEVA, risk management, or medical information is an advantage.

  • Excellent attention to detail and data accuracy.

  • Strong organizational and time management skills.

  • Ability to manage multiple projects with competing priorities.


Perks & Benefits

  • Competitive compensation package.

  • Flexible work options: Remote, Hybrid, or Office-based in Riga.

  • Inclusive and diverse team environment.

  • Clear career ladder and global advancement opportunities.

  • Ongoing professional development and training support.

  • Contribute to the safety and wellbeing of patients globally.


Company Overview

IQVIA is a global leader in advanced analytics, clinical research, and technology solutions for the life sciences industry. With operations in over 100 countries, IQVIA brings together data science, human science, and cutting-edge technology to accelerate healthcare innovation.


Work Mode

Flexible – Remote, Hybrid, or On-site (Riga, Latvia)


Call-to-Action

Ready to contribute to global patient safety and advance your career in medical information? Apply now to join IQVIA’s expert Safety Operations team and be part of a mission that truly makes a difference in public health.