Global Study Manager, Oncology R&d, Early Oncology Clinical
Zse68
Study document development and compliance
Country start-up leadership
Vendor set-up and management
As a Global Study Manager, you will turn complex protocols into operational reality, enabling decisive progress in first-in-human and proof-of-concept trials that put patients first
Job Summary
As a Global Study Manager, you will turn complex protocols into operational reality, enabling decisive progress in first-in-human and proof-of-concept trials that put patients first.
Your work will ensure study start-up, recruitment, data delivery and inspection readiness happen without delays.
Join us in our unique and ambitious world where ambition meets kindness in a community united by a clear purpose: transform outcomes for people living with cancer.
Matching Summary
As a Global Study Manager, you will turn complex protocols into operational reality, enabling decisive progress in first-in-human and proof-of-concept trials that put patients first.
Skills & Requirements
Must-have
Study document development and compliance
Country start-up leadership
Vendor set-up and management
Data delivery enablement
Financial stewardship
Investigational product supply
Operational oversight across lifecycle
Nice-to-have
Early-phase oncology trials experience
ICH-GCP and regulatory familiarity
Proficiency with clinical systems
Cross-functional team leadership
Strong analytical skills
Key Requirements
Proven experience in study document development
Experience leading country-specific document preparation
Demonstrated ability to manage third-party vendors
Experience providing input to data management documents