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

Iqvia
IQVIA
0-2 years
Not Disclosed
10 Feb. 5, 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 (Estonian & English)  

**Employer:** IQVIA  
**Location:** Tartu, Estonia  
**Salary:** Competitive  
**Start Date:** 13 Jan 2025  
**Closing Date:** 28 Feb 2025  

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### **Job Overview**  
IQVIA’s **Safety Operations team** is looking for a **Medical Information and Adverse Event Intake Specialist** fluent in **Estonian (C2/native) and English (C1+)**. This role is at the forefront of **Patient Safety**, providing direct contact with **healthcare professionals (HCPs) and patients**. You will **process safety and product quality data** and play a key role in ensuring patient well-being.  

This position offers **flexibility** – you can work **remotely, hybrid, or office-based**.  

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### **Key Responsibilities**  

- **Provide phone support** to healthcare professionals and consumers regarding **adverse events, product quality complaints, medical inquiries, and product support**.  
- **Process safety data**, including **data entry, medical terminology coding, quality control, and case closure**.  
- Document **incoming calls and emails** reporting safety concerns.  
- Foster a **positive and collaborative team environment**, mentoring **junior colleagues**.  
- Provide **regular project updates** to **Operations Team Managers** and **Customer Delivery Managers (CDMs)**.  
- Work with **Project Managers** to identify issues, propose solutions, and manage client requests.  
- Participate in **training and process improvement initiatives**.  

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### **Qualifications & Experience Required**  

- **Bachelor’s Degree in a Life Science field** (required).  
- **Fluent in Estonian (C2/native) and English (C1+ level)** (required).  
- **Experience in Lifecycle Safety** (Pharmacovigilance, CEVA, Medical Information, Risk Management, etc.) is an asset.  
- **Exceptional attention to detail and accuracy** in processing medical safety data.  
- **Ability to manage multiple projects and competing priorities**.  
- **Strong organizational and time management skills**.  

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### **Why Join IQVIA?**  
IQVIA is a global leader in **clinical research, healthcare intelligence, and life sciences**. Our mission is to **enhance patient safety, optimize medical treatments, and drive healthcare innovation**.  

🔗 **Learn more & apply:** [IQVIA Careers](https://jobs.iqvia.com)  

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