# Local Pharmacovigilance Representative - Turkey (Consultant)

> Quanticate · Turkey (Remote) · Contract · Posted 2026-04-16

**Workplace:** remote

**Department:** Pharmacovigilance

## Description

**Job Title:** Local Pharmacovigilance Representative - Turkey  
**Function:** Pharmacovigilance

**About the Role**  
We are seeking a Consultant Local Pharmacovigilance Representative in Turkey to support regulatory safety activities at a country level. This role focuses on ensuring compliance with local pharmacovigilance requirements, including safety reporting, regulatory submissions, and liaison with local health authorities.

You will play a key role in maintaining high standards of drug safety oversight while working closely with internal teams and external stakeholders.

This is a zero hour long running contract where you can expect around 10 hours of work per month starting in June so can easily fit around other contracts.

**Key Responsibilities**

**Local Regulatory Reporting**

-   Research and maintain up-to-date knowledge of local safety reporting requirements
-   Register as the Local Pharmacovigilance Representative with relevant regulatory authorities
-   Prepare and submit expedited and periodic safety reports in line with local regulations
-   Translate safety reports, regulatory documents, and correspondence from English into the local language accurately
-   Provide ongoing pharmacovigilance support to internal teams as required

**Stakeholder Collaboration**

-   Work closely with pharmacovigilance teams to ensure compliance and timely submissions to Ministry of Health, Turkish Medicines and Medical Devices Agency
-   Liaise with local regulatory authorities to understand requirements and manage submissions effectively

**Why Join**  
This role offers the opportunity to contribute directly to patient safety and regulatory compliance in a dynamic, international environment. You’ll work alongside experienced pharmacovigilance professionals and gain exposure to diverse regulatory frameworks.

## Requirements

**Knowledge**

-   Solid understanding of Turkish local pharmacovigilance reporting requirements (clinical and post-authorisation)
-   Experience with Ministry of Health, Turkish Medicines and Medical Devices Agency submissions
-   Fluency in English and the relevant local language (written and verbal)
-   A degree in pharmacy, life sciences, or a healthcare-related field is desirable

**Experience**

-   Experience working in clinical trials, either within a CRO, sponsor organisation, regulatory authority, or similar setting
-   Proven experience submitting safety reports to regulatory authorities

**Skills**

-   Strong grasp of scientific and medical terminology
-   Excellent written and verbal communication skills
-   High attention to detail and accuracy
-   Strong organisational and time management abilities
-   Proficiency in standard software tools such as Microsoft Word and Adobe Acrobat

## Benefits

-   Competitive hourly rate

## Apply

[Apply at Quanticate](https://apply.workable.com/quanticate/j/388FC79700/apply)

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