Pharmacovigilance Specialist

Abdi Ibrahim Pharmaceuticals

Abdi İbrahim, founded in 1912, has the largest product portfolio in the sector and is the largest employer in the Turkish pharmaceutical industry with 5.500 employees. Abdi İbrahim has been the leader of Turkey’s pharmaceutical industry since 2002 with its powerful vision. Today, Abdi İbrahim exports more than 70 countries. As a corporate citizen working towards creating a better world and a better future, adhering to its mission in the sector and to the requirements of societal priorities, Abdi İbrahim focuses on sustainability in all its business processes. Its vision for 2025 - apart from maintaining its status as a wholly local company - is to become "one of the top 100 pharmaceutical companies in the world. We are looking for a Pharmacovigilance Specialist. The position is located in Istanbul.

Required Qualifications

• Bachelor’s degree in Pharmacy,
• Minimum 2 years of relevant experience within a pharmaceutical company,
• Knowledge of understanding of local and global PV legislation, ICH guidance,
• Excellent command of written and spoken English,
• Good level of MS Office applications,
• Good communication skills,
• Strong organizational skills with attention to details.

Job Description

• Taking actions in the accordance with the regulations of the authority and procedures of Abdi İbrahim Pharmaceutical Companies .
• Preparing, updating, and implementing standard Pharmacovigilance operating procedures required for surveillance.
• Evaluation of all suspected adverse effects arriving to company employees including medical sales representatives.
• Collecting, recording, archiving, evaluating data about risks and safety of medicinal products and providing up-to-date data in registration files of medicinal products in this respect.
• Upon request of the authorities, fully and quickly sending response on benefit and risk balance/ratio of product, including sales or prescription volume of.
• Informing and training all employees including medical sales representatives about surveillance and responsibilities of adverse effects.
• Performing tasks and joining into projects in accordance with the supervision.