Clinical Project Manager

10 set - Ficarazzelli-bagni Italia
CROlife

Clinical Project Manager
We are looking for a Clinical Project Manager (CPM) to join our Clinical Operations team.

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Requirements: At least 4 years of experience as a Project Manager
Work Location: Rome, Italy

Key Responsibilities
- Lead, coordinate, and oversee interventional and non-interventional clinical studies involving medicinal products, medical devices, and medical nutrition.
- Manage cross-functional project teams, including Clinical Project Specialists (CPS), Clinical Trial Assistants (CTA), Clinical Research Associates (CRA), Data Managers, Medical Advisors, Biostatisticians, and external vendors.
- Ensure that clinical projects are delivered on time, within budget, and in compliance with Good Clinical Practice (GCP), applicable regulations, and company Standard Operating Procedures (SOPs).
- Prepare and oversee study documentation, including protocols, Investigator's Brochures (IB), IMPDs,



and regulatory submission packages.
- Coordinate regulatory submissions and communications with Ethics Committees and Competent Authorities.
- Monitor project progress, identify and manage risks, and provide regular updates to sponsors and internal stakeholders.
- Oversee Trial Master File (TMF) management and ensure appropriate documentation throughout the study lifecycle.
- Manage project budgets, contracts with clinical sites and external vendors, and financial performance.
- Support quality assurance activities, including CAPA implementation, KPI monitoring, and audit readiness.
- Act as the primary point of contact for sponsors and project teams throughout the duration of assigned studies.

Requirements
- Bachelor's or Master's degree in Life Sciences or a related scientific discipline.
- At least 4 years of experience as a Project Manager in the clinical research field.
- Knowledge of Good Clinical Prac

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