Director, Medical Evaluation & Case Processing Oversight
Seqirus
Multiple Locations
Global pharmacovigilance database knowledge
Medical review of icsrs
Regulatory compliance in pharmacovigilance
CSL's R&D organization is accelerating innovation to deliver greater impact for patients and is committed to developing therapies that make a meaningful difference worldwide
Job Summary
CSL's R&D organization is accelerating innovation to deliver greater impact for patients and is committed to developing therapies that make a meaningful difference worldwide.
The role involves oversight of case management processes, medical evaluation of ICSRs, driving department-wide planning, and leading transformation initiatives including vendor transitions and digital tool integration.
CSL fosters a culture of inclusion and belonging that fuels innovation and sustains a diverse workforce to advance the company and industry into the future.
Matching Summary
CSL's R&D organization is accelerating innovation to deliver greater impact for patients and is committed to developing therapies that make a meaningful difference worldwide.
Skills & Requirements
Must-have
Global pharmacovigilance database knowledge
Medical review of ICSRs
Regulatory compliance in pharmacovigilance
Case management oversight
Leadership in pharmacovigilance
Process optimization and standards development
Nice-to-have
Vendor management and coordination
Digital tools and automation pilot
Cross-functional alignment
Inspection preparation and governance
Innovation in pharmacovigilance processes
Resource and budget planning
Key Requirements
Minimum 10 years Clinical Trial and Post-marketing PV experience
At least 5 years managerial/leadership experience
BS/BA, RN, Pharmacist or similar degree
Proficient knowledge of global and local regulatory rules
Experience with global pharmacovigilance databases