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Experteer OverviewIn this role you will oversee the end-to-end TMF lifecycle for clinical trials, ensuring regulatory compliance and alignment with internal standards. You will lead the TMF Plan and Index, drive inspection readiness, and coordinate TMF activities across CROs
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
Experienced Clinical Research Associate, IQVIA Biotech - Home based, Italy 1 day ago Be among the first 25 applicants Job Overview Perform monitoring and site management work to ensure that sites are conducting the study(ies) and
The Sr CRA is an important member of the Alira Health Clinical team. The Sr CRA is highly motivated and functions independently to conduct site monitoring responsibilities for clinical trials; as well as providing oversight, leadership,
The Sr CRA is an important member of the Alira Health Clinical team. The Sr CRA is highly motivated and functions independently to conduct site monitoring responsibilities for clinical trials; as well as providing oversight, leadership,
Job Information Location Client / Employer Linical Job reference f34de96a10085eee70bcd075d0b05b5f Listing type Basic EU work permit required No Posted 19.05.2026 03.07.2026 Duties and Responsibilities Participates in the identification of potential investigative sites, conducts site qualification visits,
On behalf of our Client, Chiesi Farmaceutici, one of the top 50 pharmaceutical companies in the world with more than 80 years of experience in the pharmaceutical and biotechnology industry, IQVIA is looking for a Clinical
Job Summary Senior Chief Research Associate (Sr CRA) based in Italy, responsible for independent site monitoring, oversight, and management of clinical trials to ensure compliance with protocols, GCP, and sponsor requirements. Works closely with US and
Job Description Summary The CRA is an important member of the Alira Health Clinical team. The CRA is highly motivated and functions independently to conduct site monitoring responsibilities for clinical trials; providing oversight, leadership, and guidance
Experteer Overview In this CRA role, you will independently conduct site monitoring for clinical trials and provide guidance to the monitoring team to ensure compliance and quality. You will collaborate with cross-functional teams to address site
On behalf of our Client, Chiesi Farmaceutici, one of the top 50 pharmaceutical companies in the world with more than 80 years of experience in the pharmaceutical and biotechnology industry, IQVIA is looking for a Clinical
Project Manager (PM)The Project Manager (PM) is an important member of the Alira Health Clinical team. The PM ensures the efficient implementation of clinical study protocols, works closely with all Clinical team members, and communicates directly
As a pharmaceutical support industry leader, UBC is devoted to empowering health solutions for a better tomorrow. We take pride in improving patient outcomes and advancing healthcare. At UBC , we provide services to enhance the
The Sr CRA is an important member of the Alira Health Clinical team. The Sr CRA is highly motivated and functions independently to conduct site monitoring responsibilities for clinical trials; as well as providing oversight, leadership,
Experienced Clinical Research Associate, IQVIA Biotech - Home based, Italy 1 day ago Be among the first 25 applicants Job Overview Perform monitoring and site management work to ensure that sites are conducting the study(ies) and