We offer induction trainings in:
Pharmacovigilance Data Management Center
You will find yourself to be be supported by trainers and mentors and as the new recruit you will learn to analyse and interpret adverse event reports and the rules for recording them in the database, including evaluating report severity, using the MedDRA glossary and writing narratives. More experienced specialists are provided with an opportunity to get more advanced training in modules such as medical literature, advanced Pharmacovigilance processes and accessing the EudraVigilance database. All this is performed in an international setting, in close cooperation with equivalent departments in China, Columbia and Costa Rica.
Clinical Trials Data Management Center
You will spend first three months with qualified trainers, mentor support and access to a comprehensive online training platform. This time is intended for you to be used for learning about data management from clinical trials, Good Clinical Practice principles and the databases, systems and tools available.
For more experienced individuals the programs include training in specific therapeutic areas, writing and following (SOP) procedures and access to the SCDM platform (Society for Clinical Data Management).
For the most experienced employees, we provide a global certification program and knowledge development initiatives through participation in international conferences and meetings with specialists from our Clinical Trial Data Management Centres (the Americas, Asia).