Lead and coordinate a cross-functional study team to ensure clinical study progress according to timelines, budget, and quality standards
Job Summary
Lead and coordinate a cross-functional study team to ensure clinical study progress according to timelines, budget, and quality standards.
Serve as the primary point of contact for CRO Project Managers to ensure study delivery while maintaining appropriate oversight throughout the study lifecycle.
Ensure all studies are inspection-ready at all times in accordance with ICH-GCP and company policies.
Matching Summary
Lead and coordinate a cross-functional study team to ensure clinical study progress according to timelines, budget, and quality standards.
Skills & Requirements
Must-have
7 years clinical R&D experience
2 years project management experience
ICH-GCP and AZ SOP compliance
CRO oversight and management
Study budget forecasting and control
Risk-based quality management
Trial Master File (TMF) oversight
Nice-to-have
Mentoring less experienced colleagues
Leading process improvement projects
Strong conflict management skills
Strategic critical thinking abilities
Experience with non-drug projects
Key Requirements
University degree in medical or biological sciences
7 years relevant clinical experience in pharmaceutical industry
2 years project management experience
Right to work in advertised country/ies
Work Rights
Must have right to work in country where role is advertised