Clinical Trial Project Manager

Overview In this role you will coordinate the operational management of assigned clinical trials to ensure timely, on-budget delivery compliant with ICH GCP and Chiesi SOPs. You will liaise with multiple stakeholders and manage study budgets and invoicing, contributing to global programs. You will provide operations input during study design, act as a primary contact for customers, and support documentation, budgeting, and quality systems initiatives. This position offers cross-functional collaboration across a global team and opportunities to shape rare-disease trials.

Retribuzione / Benefits

pension

private medical insurance

wellbeing programme

flexible benefits programme

relocation support

remote work options

Responsabilità

Coordinate operational management of assigned clinical trials per ICH GCP and SOPs

Communicate with multiple stakeholders during study progression

Manage budgets and invoices for study payments

Proactively manage study timelines, budgets, and resources with core team

Make operational decisions to initiate and complete global trials on time and in scope

Provide clinical operations input during study design and planning

Serve as primary contact for internal/external customers

Prepare and archive study-specific documents

Coordinate input from internal departments to ensure SOP compliance

Support budget computation and control for studies/programs

Support Global GRD QMS for SOPs and related projects

Requisiti fondamentali

• Bachelor's degree in Life Sciences or equivalent
• Five+ years clinical research experience
• 3+ years global clinical project management experience
• Knowledge of ICH/GCP principles and study design
• Strategic thinking
• Project and Program Management
• Cost/Benefit Analysis
• Proficiencies in Microsoft Applications (Word, Excel, PPT)
• Stakeholder management
• Effective communication
• Cross-functional collaboration
• ICH/GCP knowledge
• Clinical trial planning and design
• Budgeting and cost control