A global leader in clinical research services is seeking a Clinical Research Associate in Milan, Italy. The role involves performing site monitoring, supporting subject recruitment, and ensuring compliance with regulatory standards. Candidates should have a Bachelor's and Master's degree in a relevant field, CRA certification, and experience in the Pharma industry. This full-time position offers...
A global clinical research organization is seeking a Senior Clinical Research Associate (CRA) to oversee clinical trials and ensure compliance with regulatory standards. The successful candidate will have extensive experience in clinical trial processes and strong organizational skills. Responsibilities include monitoring sites, conducting visits, and collaborating with teams. This role offers...
Experienced Clinical Research Associate, IQVIA Biotech - Home based, Italy page is loaded## Experienced Clinical Research Associate, IQVIA Biotech - Home based, Italylocations: Milan, Italytime type: Full timeposted on: Posted Todayjob requisition id: R1501739Job Overview:Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as...
Social network you want to login/join with:CliniRx has a number of CRA positions available to support a global study in Q1 2025.We are expanding rapidly and offer multiple permanent opportunities to join us on a global study. Ideally, candidates will come from a CRO background with experience across multiple therapeutic areas.As a global contract research organization (CRO), we provide a diverse...
Location : located in North Italy; MilanWho we areOptimapharm is a globally operating leading mid‐size full‐service CRO aiming to deliver new therapies to improve and save patients lives.Optimapharm's key priorities are the well‐being of our people, consistent quality delivery to our clients and healthy sustainable growth.With 26 strategically located offices Optimapharm operates in 40 countries,...
Location: located in North Italy; MilanWho we are?Optimapharm is a globally operating, leading, mid-sized, full-service CRO aiming to deliver new therapies to improve and save patients' lives.Optimapharm' s key priorities are the well-being of our people, consistent quality delivery to our clients and healthy, sustainable growth.With 26 strategically located offices, Optimapharm operates in 40+...
A leading global provider of clinical research services is seeking an Experienced Clinical Research Associate to monitor and manage clinical study sites based in Italy. The ideal candidate will have a Bachelor's degree and a Master's degree in a scientific field or health care, along with CRA certification. The role involves ensuring regulatory compliance, managing documentation, and maintaining...
Experienced Clinical Research Associate, IQVIA Biotech - Home based, Italy page is loaded## Experienced Clinical Research Associate, IQVIA Biotech - Home based, Italylocations: Milan, Italytime type: Full timeposted on: Posted Todayjob requisition id: R1501739Job Overview:Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as...
Clinical Research Associate, Sponsor Dedicated – ItalyJoin to apply for the Clinical Research Associate, Sponsor Dedicated – Italy role at IQVIAResponsibilitiesPerforming site selection, initiation, monitoring and close‐out visitsSupporting the development of a subject recruitment planEvaluating the quality and integrity of site practices in accordance with regulatory requirements, i.E., Good...
Experienced Clinical Research Associate, IQVIA Biotech - Home based, Italy1 day ago Be among the first 25 applicantsJob OverviewPerform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements.Essential FunctionsPerform site monitoring visits...
A global clinical research provider is seeking a Site Manager to oversee monitoring activities in clinical trials. Responsibilities include conducting site visits, ensuring regulatory compliance, and collaborating with study sites. The ideal candidate will have a Bachelor's and Master's degree in relevant fields, CRA certification, and experience in the pharma industry. Excellent English skills...