MINIMUM REQUIRED EDUCATION AND EXPERIENCE
· Bachelor’s degree in a life-science, medicine, pharmacy or nursing or educational equivalent.
· 3 years of prior relevant experience including experience managing clinical trial safety/post-marketing safety; or equivalent combination of education, training and experience.
· Excellent written and verbal skills in English (min. C1) and Estonian language (min. C2 / native).
• In-depth knowledge of applicable global, regional and local regulatory requirements, International Conference on Harmonization (ICH) guidelines, and relevant Standard Operating Procedures (SOPs).
• Very good knowledge of the pharmacovigilance legal framework in Estonia.
• Maintain an overview of the safety profile of the product and factors that may affect the benefit/risk balance of a product.
• Demonstrate an understanding of compliance and of quality management systems.