GENERAL INFORMATION
Location: Porto/Heidenheim an der Brenz/Berlin or remote (Portugal/Germany)
Starting: at the next possible date
YOUR PROFILE
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 keeping up to date with new developments in pharmacovigilance ensures you – and us – stay on course.
- You possess the ability to implement applicable laws into our and our customers’ processes and policies swiftly.
- Your medical knowledge enables you to handle adverse drug reactions and medical inquiries effectively.
- You want to work in the field of medical affairs and feel comfortable engaging with professionals within the medical community.
- Your organizational talent and time management skills are exceptional.
- A proficiency in English and German (both written and spoken) allows for effective communication with our team and customers.
YOUR TASKS
YOUR ONGOING MISSION:
- Building systems and processes that enable our clients to conduct effective PV activities, and monitoring the performance and compliance of PV systems.
- You lead, coordinate, and support PV audits and inspections.
- Medical writing is familiar territory for you, allowing you to prepare PV documents throughout the entire lifecycle of our customers’ products.
- Tasks such as Medical Literature Monitoring, Signal Management, ICSR Management, and SUSAR Management are within your scope or are areas where you are eager to develop further.
- You are familiar with the universe of Quality Management Systems in PV and managing Standard Operating Procedures (SOPs), ensuring they are up-to-date and effective.
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Kontaktperson:
THE FORCE CT GmbH HR Team