IQVIA Safety Operations team play an important part in the design, build and execution of end-to-end safety solutions for major pharmaceutical companies and their post market products around the world. We are proud to be an international, diverse team based across the world, with ‘safety hubs’ in Ireland, Poland, Austria, Portugal, Slovakia, Spain, India and USA. Each new joiner is supported by a nurturing management team, collaborative colleagues as well as a clear career ladder with plenty of opportunities to allow you to grow, adapt and shine.

　　We are looking for the best talent, with English language expertise to be part of a global team that partnership with a major pharmaceutical company, working with patient safety on post-market products. Apply your knowledge and expertise, including complex decision making, to review, assess and process safety and product quality information.

　　Adverse Event Intake Specialist with English and Turkish language

　　Summary :

　　Review, assess and process safety data and information, across service lines, received from various sources and distribute reports/data onwards to both internal and external third parties, following applicable regulations SOPs and internal guidelines under guidance and support of senior operation team members.

　　Key responsibilities:

　　To Prioritize and complete the assigned trainings on time.

　　Receiving, reviewing and interpretation of medical report.

　　Process safety data according to applicable regulations, guidelines, Standard Operating procedures (SOPs) and project requirements.

　　To perform Pharmacovigilance activities per project requirement including but not limited to, collecting and tracking incoming.

　　AdverseEvents(AE)/endpoint information.

　　Determining initial/update status of incoming events.

　　Database entry.

　　Coding AE and Products, writing narratives, Literature related activities as per internal/ project timelines.

　　Ensure to meet quality standards per project requirements.

　　Ensure to meet productivity and delivery standards per project requirements.

　　To ensure compliance to all project related processes and activities.

　　Creating, maintaining and tracking cases as applicable to the project plan.

　　Identify quality problems, if any, and bring them to the attention of a senior team member.

　　To demonstrate problem solving capabilities.

　　Attend project team meetings and provide feedback to operations manager on any challenges/issues or successes.

　　100% compliance towards all people practices and processes.

　　Minimum Required Education and Experience

　　Must be Native/C2 level Turkish and fluent in English language (min. C1)

　　Bachelor’s Degreein Pharmacy is a must

　　Skills and Abilities

　　Excellent attention to detail and accuracy.

　　Good knowledge of medical terminology.

　　Self-motivated and flexible.

　　Ability to follow instructions/guidelines, utilize initiative and work independently.

　　IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. Learn more at https://jobs.iqvia.com

　　IQVIA is a world leader in using data, technology, advanced analytics, and expertise to help customers drive healthcare – and human health – forward. Together with the companies we serve, we are enabling a more modern, more effective and more efficient healthcare system, and creating breakthrough solutions that transform business and patient outcomes.

　　To get there, it takes diverse skills and a curiosity to explore new possibilities. No matter your role, everyone at IQVIA, including our colleagues at Q² Solutions, contributes to our shared goal of improving human health. Thank you for your interest in growing your career with us.

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