Your mission
At AiCuris, the role of the Pharmacovigilance Officer is of the highest importance. Bringing broad knowledge to the drug safety function, you are embedded into AiCuris project teams and support drug development related to all aspects of pharmacovigilance during discovery, drug development, regulatory review and approval. One of the long-term goals of this role is to extend the AiCuris drug safety function towards a marketing authorization holder.
Responsibilities
- Responsible for all drug safety aspects within development and future marketed new drugs
- Overseeing the risk-benefit profile of all drugs under development
- Being the contact for regulatory agencies related to safety as well as the primary contact for PV inspections in Europe
- Taking over EU-QPPV responsibility as well as the Graduated Plan Officer (Stufenplanbeauftragter (m/w/d)) function at AiCuris as needed in the future
- Implementing and maintaining the pharmacovigilance system and establishing its system master file
- Ensuring adherence to the GVP modules as defined by the European Commission
- Continuous observation of the regulatory landscape and scientific literature regarding pharmacovigilance
- Reviewing and amending safety information within development documents
- Responsible for writing and reviewing adverse event narratives and periodic reports
- Responsible for standard operating procedures in pharmacovigilance, regular updates and training adherence
- Overseeing service providers