Experience

Botanik Eczanesi

• Türkiye
• Pharmaceutical Manufacturing
• 1 - 100 Employee

• Pharmacy Owner

  • Aug 2020 - Present

  Achieved a significant growth in pharmacy revenue within 3 years, while simultaneously doubling the size of the team. Accountable for overseeing a team of 3 pharmacists and 1 pharmacy technician, ensuring their motivation and engagement levels are maintained. Strategically plan and implement yearly and quarterly sales strategies, aligning them with employee KPIs. Remain vigilant in adhering to legal and ethical standards within the pharmacy setting. Establish quality control checkpoints throughout the pharmacy operations. Foster and cultivate partnerships with new stakeholders, while nurturing existing relationships to meet their needs and maintain quality standards. Effectively handle inventory management and supply chain operations. Provide pharmacy management training to team, e.g P&L & Category Management. Show less



GSK

• United Kingdom
• Pharmaceutical Manufacturing
• 700 & Above Employee

• Regional Medical Content Executive

  • Jan 2019 - Aug 2020

  Member of emerging market medical content hub as medical review and final signatory for Turkey, Saudi and Gulf across several therapeutic area, mainly working with country medical and commercial team as well as above country teams. Reported directly to Head of EM Medical Content Hub.

• Pharmacovigilance Executive

  • Feb 2017 - Jan 2019

  Responsible of all PV activities GSK Turkey pharma, vaccine portfolio and back up for Consumer Health. Executed management monitoring and due diligence activities promptly, including vendor system control.



AIFD | Araştırmacı İlaç Firmaları Derneği

• Türkiye
• Pharmaceutical Manufacturing
• 1 - 100 Employee

• Vice President for PV Group in AİFD

  • 2018 - 2019

  - Working as Vice president in the pharmacovigilance working group - Constant communication with MoH on behalf of AİFD PV working group - Creation of PV data privacy guidance within the working group - Organizing and leading the meetings - Working as Vice president in the pharmacovigilance working group - Constant communication with MoH on behalf of AİFD PV working group - Creation of PV data privacy guidance within the working group - Organizing and leading the meetings



Merck Türkiye

• Türkiye
• Pharmaceutical Manufacturing
• 1 - 100 Employee

• Drug Safety Associate

  • Jun 2015 - Feb 2017

  - Adverse event management from all sources (spontaneous, PSPs, etc) - Maintain and update the Local PV file quarterly. - Handle all reconciliation process with PSP/Local departments/Vendor/Medical information - Safety control of SmPC, PIL documents before validation submission. - Medical information management though OneGMI system. - Adverse event management from all sources (spontaneous, PSPs, etc) - Maintain and update the Local PV file quarterly. - Handle all reconciliation process with PSP/Local departments/Vendor/Medical information - Safety control of SmPC, PIL documents before validation submission. - Medical information management though OneGMI system.



Dem İlaç

• Türkiye
• Pharmaceutical Manufacturing
• 100 - 200 Employee

• Pharmacovigilance & Regulatory Affairs Associate

  • Jul 2014 - Jun 2015

  - Management of ICSR reporting and submission of all the needed reports to HA in accordance with local regulations for import and export products. - Preparation of PBRERs for export products - Distribution of dear health care professional letter. - Preparation of CTD dossiers for import and local products. - Perform necessary variations, analyses application and GMP applications. - Control all artworks and make sure that the artworks are confirm with TR MoH requirements - Management of ICSR reporting and submission of all the needed reports to HA in accordance with local regulations for import and export products. - Preparation of PBRERs for export products - Distribution of dear health care professional letter. - Preparation of CTD dossiers for import and local products. - Perform necessary variations, analyses application and GMP applications. - Control all artworks and make sure that the artworks are confirm with TR MoH requirements