Job Purpose We’re looking for a highly organized and detail‑oriented TMF Specialist to join our Clinical Operations team and play a key role in ensuring excellence across our clinical documentation processes. In this role, you will be
Experteer Overview In 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
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
Job Purpose We’re looking for a highly organized and detail‑oriented TMF Specialist to join our Clinical Operations team and play a key role in ensuring excellence across our clinical documentation processes. In this role, you will be
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
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
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 Description Summary Job Description ROLE The Project Manager (PM) is an important member of the Alira Health Clinical team. The PM ensures the efficient implementation of one or more study protocols, works closely with all
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
Nouscom is a private clinical stage immuno-oncology company developing next-generation, off-the-shelf and personalized cancer vaccines. Our proprietary viral vector platform has the capacity to encode for large payloads of neoantigens or other immunomodulators and is clinically
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
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 entire
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
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
Experteer OverviewIn 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 questions,
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
Job InformationLocationClient / EmployerLinicalJob referencef34de96a10085eee70bcd075d0b05b5fListing typeBasicEU work permit requiredNoPosted19.05.202603.07.2026Duties and ResponsibilitiesParticipates in the identification of potential investigative sites, conducts site qualification visits, collects, and reviews site regulatory documents, and prepares site qualification visit reports and associated
Job SummarySenior 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 EU
Job Description SummaryThe 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 in
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