Senior Global Process Owner - Study & Site Management
Novartis
Dublin, Ireland
Hybrid
End-to-end clinical trial process management
Regulatory compliance in clinical trials
Process improvement and automation
As Senior Global Process Owner for Study & Site Management you will own the end‑to‑end, regulatory‑compliant study and site process, strengthening its health and maturity through continuous improvement, and powering faster, quality‑driven clinical delivery that gets transformative medicines to patients sooner
Job Summary
As Senior Global Process Owner for Study & Site Management you will own the end‑to‑end, regulatory‑compliant study and site process, strengthening its health and maturity through continuous improvement, and powering faster, quality‑driven clinical delivery that gets transformative medicines to patients sooner.
The Senior Global Process Owner acts as a single point of ownership that drives process health and continuous improvement for sustained process maturity.
You will be an advocate for simplification and process automation while collaborating across global line functions within a complex matrix.
Matching Summary
As Senior Global Process Owner for Study & Site Management you will own the end‑to‑end, regulatory‑compliant study and site process, strengthening its health and maturity through continuous improvement, and powering faster, quality‑driven clinical delivery that gets transformative medicines to patients sooner.
Skills & Requirements
Must-have
End-to-end clinical trial process management
Regulatory compliance in clinical trials
Process improvement and automation
Cross-functional collaboration
Governance and risk management
Site management and clinical trial monitoring
Nice-to-have
Strategic process planning
Process simplification and optimization
Quality documentation improvement
Change management initiatives
Process mapping coordination
Key Requirements
University degree in Life Science, quantitative science or business
5 years' experience in Site Management or Clinical Trial Monitoring
Extensive knowledge of clinical development processes and regulations
Experience in process improvement and operational planning
Desirable qualifications in project management, 6-Sigma, Lean, MBA