Global Study Manager, Oncology R&d, Early Oncology Clinical
Trzdev35
Study document development and compliance
Country start-up leadership
Vendor set-up and management
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
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.
When urgent opportunities arise, we mobilize quickly—turning ideas into well-designed trials and actionable data in weeks, not months.
Matching Summary
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 global regulatory knowledge
Proficiency with clinical systems
Cross-functional team leadership
Strong analytical skills
Key Requirements
Proven experience contributing to study document development
Experience leading country-specific agreements
Demonstrated ability to set up and manage third-party vendors
Experience providing input to data management documents
Capability to initiate contract and budget requests