05 ago
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Biotecnologie - Farmacia - Chimica
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Italia
05 ago
Biotecnologie - Farmacia - Chimica
Italia
ID: 2525
Date of Posting: Apr 27, 2026
Business Area: Research & Development
Job Type: Direct Employee
Territory:
Full-Time or Tempo parziale: Full Time
Seniority: Mid-senior
With its beginnings in a family run pharmacy in Correggio, Italy in the 1920s, Recordati is now a global pharmaceutical company, listed on the Italian stock exchange, with over 4,500 employees and turnover of over Euro 2bn.
We are a group of like-minded, passionate individuals who go to extraordinary lengths for our patients, customers, partners, investors and the people across the globe who we serve. We develop and commercialise medicines to serve people living with common diseases, as well as those living with some of the rarest, in around 150 countries.
At Recordati, our mantra is simple. We've always believed that health, and the opportunity to live life to the fullest, is a right, not a privilege. Whether that is for common diseases or the rarest – we want to give people the opportunity to be the best version of themselves.
This drive will never stop. Together,
we will always be reimagining tomorrow – with new ideas, new technologies and new innovations to fight diseases.
Recordati. Unlocking the full potential of life.
Job Purpose
The Clinical Trial Liaison Manager (CTLM) is responsible for site performance, trial delivery and Sponsor oversight across assigned countries. The CTLM ensures timely, high‐quality clinical trial execution, with a strong focus on patient recruitment, protocol adherence, regulatory compliance, and data quality. Acting as the primary Sponsor representative ("face of Recordati") at site level, the CTLM builds and maintains strong relationships with Principal Investigators (PIs) and site teams, supports study start‐up and recruitment, and provides in‐field oversight of CRO activities—particularly CRA performance—as part of Recordati's Sponsor oversight responsibilities. The CTLM serves as a key escalation point for site and investigator issues, including unresolved CRO m
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