Pharmacovigilance / PV Manager (m/w/d) Porto, Heidenheim a. d. Brenz/Berlin/remote

YOUR EQUIPMENT FOR THIS JOURNEY:

• Practical knowledge of PV processes and concepts, including national, European, and global directives, regulations, and guidelines (ICH, GVP, GCP, etc.) allows you a smooth launch.  
• Your dedication to keep up to date with new developments in the field of pharmacovigilance keeps you – and us – on course.
• You possess the ability to implement applicable laws into our and our customers’ processes and policies at lightspeed.
• Your medical knowledge transports you to a place where you know how to deal with adverse drug reactions and medical enquiries.
• You want to work in the field of medical affairs and don’t feel like an alien when engaging with players within the medical community.
• Your organization talent and time management skills are almost out of this world.
• A proficiency in English and German (written and spoken alike) allows you to effectively communicate with our team and customers.

YOUR ONGOING MISSION:

• Building systems and processes that allow our clients to run effective PV activities is part of your mission as well as monitoring the performance and compliance of PV systems.
• You lead, coordinate, and support PV audits and inspections.
• Medical Writing doesn’t make you feel like you’re from a different planet, allowing you to preparing PV documents through the entire lifecycle of our customers’ products.
• Tasks like Medical Literature Monitoring, Signal Management, ICSR Management, and SUSAR Management aren’t unidentified objects to you – or you are ready for further development in any of these spheres.
• You’re familiar with the universe of Quality Management Systems in PV and managing Standard Operating Procedures (SOPs) and take care of them, as well.