Senior Pharmacovigilance Specialist
Cencora Посмотреть все вакансии
- Киев
- Постоянная работа
- Полная занятость
- Data entry and quality control of Individual Case Safety Reports (ICSR) of adverse drug reactions deriving from clinical trials, spontaneous reporting systems and the literature; reporting of ICSRs to the competent authorities
- Support in the generation, processing, documenting, and tracking of follow-up requests
- Screening and documentation of scientific literature regarding safety relevant publications
- Assist in the creation of periodic reports PSURs (Periodic Safety Update Reports), DSURs (Development Safety Update Reports), PADERs (Periodic Adverse Drug Experience Reports), risk management plans and signal detection reports
- Interact with customers as needed (e.g. meetings, client visits, day to day case processing, etc.)
- PSMF maintenance
- Contribute to/review QA documents such as Working Instructions, SOPs, Working Procedures, templates, project metafiles, etc. for pharmacovigilance projects
- Prepare for and participate in internal and external audits/inspections
- Training new colleagues in relevant tasks
- The employee agrees to take over primary listed tasks and responsibilities in other service lines, project management activities as client contact point and additional reasonable tasks that align with their abilities, qualification and training, if required.