In collaboration with the other Pharmacovigilance (PV) staff members, you will support activities related to pharmacovigilance, to ensure that all aspects of the local system are compliant with corporate and legal requirements.
On a daily basis you will be responsible for the handling of reporting of Adverse Events:
Depending on the workload in the PV team and the profile of the candidate, this function may also be involved in other PV activities, such as training, procedures, periodic safety reports, compliance monitoring, changes in legislation, literature screening, agreements with service providers, audits and inspections, risk management, updates in product safety information, local studies,...
This function may occasionally also be involved in activities related to Regulatory Affairs and Quality Assurance to support other functions within the department.
We offer a fulltime contract, including competitive salary and advantages.
Furthermore, you will be able to expand your horizon by participating in different projects.
For more infomation contact Marieke Franken on+32472455816 or email@example.com