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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📌 Clinical Trial Liaison Manager (Milano)
🏢 Altro
📍 Milano