Clinical Trial Liaison Manager
Pubblicato il 31-07-2026 - Altro in Milano
Experteer Overview As a CTLM, you act as Recordati's sponsor representative at site level, driving trial delivery and strong PI/site partnerships. You will support site start-up, recruitment, and Sponsor oversight of CRO activities to ensure compliant, high-quality trial conduct. You contribute to data integrity, regulatory adherence, and issue resolution while liaising with cross-functional teams. This role offers exposure to global trials, patient recruitment strategies, and site performance optimization in a mission-driven pharma environment. You will help position Recordati as a sponsor of choice by maintaining proactive, solutions-oriented site engagement.
Retribuzione / Benefits Sponsor ambassador at site level, building long-term PI/site staff relationships
Drive patient recruitment by engaging with PIs and optimizing enrolment plans
Collaborate with CRAs/site coordinators to align recruitment and site priorities
Foster cross-department collaboration at trial sites to improve patient identification and enrolment
Monitor recruitment metrics and proactively mitigate enrolment risks
Provide Sponsor oversight of CRO monitoring, focusing on CRA performance and adherence to processes
Conduct Sponsor Oversight Visits (SOVs) and study progress visits for compliant monitoring
Attend PSVs, SIVs, IMVs and COVs as defined with the Lead CSM
Deliver motivational visits to re-energise site engagement and performance
Ensure data quality and integrity through on-site and remote review in line with ICH GCP and local regulations
Identify operational and site-level issues, escalation risks appropriately, and drive timely resolution
Maintain accountability for long-term site partnerships with actionable insights for the study team
Establish regular PI engagement to discuss study progress and recruitment plans
Report site status, performance insights, risks, and mitigations to Lead CSM
Work across multiple trials to ensure consistent Sponsor presence and oversight
Responsabilità Minimum 6 years' experience in Pharma/Biotech, preferably in clinical site monitoring, oversight or engagement
Strong understanding of healthcare landscape, patient pathways and site operations
Proven ability to build and manage relationships with PIs, site staff, CROs and internal stakeholders
Demonstrated proactive leadership and ability to influence without authority
Organisational, analytical and problem solving skills with strong prioritisation
Experience with clinical trial systems and tools (CTMS, eTMF, EDC)
Experience in global clinical trials; rare disease experience is a strong advantage
Valid driver's licence
Fluent written and spoken English, Polish and/or Romanian
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