Medical Evaluation & Case Processing Oversight Lead

Medical Evaluation & Case Processing Oversight Lead

You will oversee all areas of single case processing in the global pharmacovigilance database from all sources. This includes ensuring that the vendor performs case processing in accordance with regulatory guidelines, PV agreements, and the Company's SOPs, as well as responding to specific questions or queries about cases. This role develops standards and processes, with a focus on global compliance and process optimization.

Oversees Medical Evaluators responsible for medical review of ICSR.

• Oversight of Case Management Processes activities
• Oversight of Medical Evaluator role which completes medical review of the following ICSR:
  All serious cases from all sources
• Non-serious cases from company-sponsored clinical study, if required
• Legal ICSR (serious and non-serious)
• Reportable cases of combination products with device issue(s) / malfunction (serious and non-serious)
• Non-serious ICSR processed by Case Managers and reviewed for correct seriousness on an aggregate basis by Medical Evaluator
• Drive department-wide planning: resource, budget, and organisational strategy
• Own case management dashboards and governance scorecards
• Prepare for internal and external inspections, including coordination of creation of presentations
• Lead transformation initiatives (e.g., vendor transitions, digital tools)
• Monitor regulatory trends and represent PV case management in global initiatives
• Coordinate departmental leadership meetings and communication
• Pilot innovations (e.g., RPA, AI triage, tech integration)
• Align with Clinical, QA, Regulatory, and Safety Science functions
• Coordinate creation and update of SOPs
• Retain product and process knowledge

• Review of seriousness, listedness and causality assessments
• Review of event terms and MedDRA coding
• Review of narrative for medical accuracy and consistency
• Assessment of the need for Quality Investigations
• Generation of medical follow-up queries / Targeted Questionnaires

• Minimum of 10 years of Clinical Trial and Post‑marketing Pharmacovigilance (PV) experience with 5 years of managerial/leadership experience
• Global pharmacovigilance database knowledge is required along with proficient knowledge of global and local regulatory rules and regulations

• BS/BA, RN, Pharmacist, or similar

CSL Behring is a global biotherapeutics leader driven by our promise to save lives. Focused on serving patients’ needs by using the latest technologies, we discover, develop and deliver innovative therapies for people living with conditions in the immunology, hematology, cardiovascular and metabolic, respiratory, and transplant therapeutic areas. We use three strategic scientific platforms of plasma fractionation, recombinant protein technology, and cell and gene therapy to support continued innovation and continually refine ways in which products can address unmet medical needs and help patients lead full lives.

CSL Behring operates one of the world’s largest plasma collection networks, CSL Plasma. Our parent company, CSL, headquartered in Melbourne, Australia, employs 32,000 people, and delivers its lifesaving therapies to people in more than 100 countries.

For more information on CSL benefits visit How CSL Supports Your Well‑being | CSL.

CSL is an Equal Opportunity Employer. If you are an individual with a disability and need a reasonable accommodation for any part of the application process, please visit

• Director

• Full‑time

• Other