Clinical Trial Supply Lead: Global Impact & Innovation

Novartis; Basel; Vor Ort; CHF 94.000 - 174.000; Vollzeit

Zusammenfassung

Novartis in Basel, Switzerland is seeking a Clinical Trial Supply Manager to define and execute an optimal supply strategy for clinical trials, ensuring continuous patient supply. You will lead end-to-end planning for diverse studies and manage GMP systems and external vendors.

The role requires advanced degrees in life sciences with 5+ years of experience in clinical supplies, strong project management, and data-driven decision making. Onsite with hybrid options where possible.

Qualifikationen

• Masters or Doctorate in life sciences with 5+ years in clinical supplies.
• Strong operation excellence, planning, and attention to detail.
• Experience with data/digital innovations to enhance outcomes.
• GMP processes knowledge is desirable.

Aufgaben

• Lead study supply to ensure timely planning and execution of supply strategy for continued supply of clinical finished goods to patients.
• Develop end-to-end clinical supplies for diverse studies, including traditional and innovative setups for advanced therapies.
• Provide inputs in study protocols and design for optimal supply strategy and risk-based planning.
• Design patient-centric packaging and distribution plans for all trial phases.
• Independently manage IRT, packaging, and distribution vendors throughout the study duration.
• Use GMP planning systems (SAP and IRT) for cross-functional planning of resources and clinical supplies.
• Serve as SPOC for Global Clinical Supply at trial level for the Clinical Trial team.

Kenntnisse

SAP

IRT

Clinical supply

Project management

Data analytics

GMP knowledge

Ausbildung

Masters or Doctorate in life sciences

MBA with bachelor’s degree

Tools

SAP

IRT

Jobbeschreibung

Novartis in Basel, Switzerland is seeking a Clinical Trial Supply Manager to define and execute an optimal supply strategy for clinical trials, ensuring continuous patient supply. You will lead end-to-end planning for diverse studies and manage GMP systems and external vendors.

The role requires advanced degrees in life sciences with 5+ years of experience in clinical supplies, strong project management, and data-driven decision making. Onsite with hybrid options where possible.