Novartis
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Biotech • Pharmaceutical
Leads GCP compliance across an EMEA clinical operations hub, overseeing quality issues, audits, inspections, investigations, CAPA, risk management, and inspection readiness. Manages and develops a high-performing compliance team while partnering with clinical operations, Quality Assurance, and senior leadership to strengthen regulatory compliance, operational excellence, and sustainable quality outcomes across clinical trials.
Biotech • Pharmaceutical
Provides legal counsel for pharmaceutical research and development across the UK and EMEA. Advises on clinical trials, regulatory requirements, data use, patient-focused research, emerging technologies, and AI adoption. Drafts and negotiates research, development, collaboration, and commercial agreements while supporting external innovation and asset integration. Partners with scientists and business leaders to manage legal risk, improve processes, and enable compliant innovation.
Biotech • Pharmaceutical
Provides clinical and scientific support across clinical study phases, including patient-level data review, trend analysis, data quality management, issue resolution, protocol compliance, and safety review. Supports data review plans, case report forms, regulatory documents, clinical study reports, training, and study meetings. Collaborates with cross-functional teams to identify clinical insights, protect patient safety, maintain data integrity, and improve clinical data review processes.
