The role involves leading a cross-functional team to ensure clinical study progress aligns with timelines, budget, and quality standards
Job Summary
The role involves leading a cross-functional team to ensure clinical study progress aligns with timelines, budget, and quality standards.
Candidates must maintain strict oversight of external service providers and CROs while ensuring all documentation meets AZ SOPs and ICH-GCP guidelines.
The position requires accountability for study budget re-forecasting and managing financial risks throughout the entire study lifecycle.
Matching Summary
The role involves leading a cross-functional team to ensure clinical study progress aligns with timelines, budget, and quality standards.
Skills & Requirements
Must-have
Lead cross-functional study teams
Manage CRO oversight and delivery
Develop clinical study protocols
Ensure ICH-GCP compliance
Manage study budgets and forecasting
Oversee Trial Master File completion
Nice-to-have
Mentor less experienced colleagues
Drive process improvement projects
Strong conflict management skills
Strategic critical thinking abilities
Key Requirements
University degree in medical or biological sciences
7 years relevant clinical experience in pharmaceutical industry
2 years project management experience
Extensive knowledge of clinical research regulatory requirements
Work Rights
Must have right to work in the country/ies where the role is advertised