The Global Study Associate Director is accountable for the delivery of clinical studies by leading a cross-functional study team and ensuring successful study delivery according to timelines, budget, and quality standards
Job Summary
The Global Study Associate Director is accountable for the delivery of clinical studies by leading a cross-functional study team and ensuring successful study delivery according to timelines, budget, and quality standards.
Responsibilities include leading study teams, managing budgets, overseeing external service providers, ensuring regulatory compliance, and maintaining inspection readiness.
The role involves providing feedback on individual performance to study team members and their line managers to support professional development.
Matching Summary
The Global Study Associate Director is accountable for the delivery of clinical studies by leading a cross-functional study team and ensuring successful study delivery according to timelines, budget, and quality standards.
Salary
Base: 217.800,00 zł - 521.000,00 zł; Bonus/Equity: Not specified; Benefits: Not specified
Skills & Requirements
Must-have
Clinical study delivery
Cross-functional team leadership
Clinical trial regulations ICH GCP
Study budget management
Vendor oversight
TMF completion oversight
Nice-to-have
Strategic thinking abilities
Problem-solving skills
Conflict management skills
Professional development support
Key Requirements
7 years relevant clinical experience
2-4 years global project management experience
Experience in all phases of clinical study lifecycle
Experience with imaging or lab vendors
University degree in medical or biological sciences