Un importante ospedale di ricerca a Milano cerca un Data Manager per il progetto 'Prehabilitation to improve heart Rate variability In surgical cancer patients'. Il candidato si occuperà della gestione dei dati, redazione di report e inserimento delle informazioni cliniche. È richiesta laurea magistrale in Biologia o titolo equivalente e si offre un contratto di collaborazione con un trattamento...
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...
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...
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...
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,...
Company DescriptionPSI is a leading Contract Research Organization with more than 30 years in the industry, offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications.Job DescriptionAs aClinical Research Associateat PSI Italy you will enjoy a variety of monitoring tasks...
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 healthcare organization in Italy is seeking a Senior Contract Analyst to manage contractual agreements and ensure compliance with regulations. You will collaborate with internal stakeholders, analyze contract terms, and provide guidance to project teams. The ideal candidate has a Bachelor's degree in business or legal studies, and experience in contract negotiation. ICON offers...
L'IRCCS Ospedale San Raffaele (OSR), struttura clinica-scientifica-universitaria di rilievo internazionale e di alta specializzazione per diverse importanti patologie, sta ricercando un Study Coordinator/Data Manager da inserire nella propria Unità/Laboratorio URI-Urological Research Institute.Attività principaliGestione di database di pazienti: raccolta, data entry e collaborazione...
Job SummaryMedpace is the leading CRO for Biotech companies and is continuing to add Clinical Trial Managers of different experience levels to join our Clinical Trial Management Group in our Milan office. Clinical Trial Managers with expertise in Immunology and Infectious Diseases are welcome to continue to work in their area of expertise or to expand to a new therapeutic area.We provide remote...
Job SummaryThe Sr. Manager, Clinical Development Scientist:Is accountable for the scientific integrity of the study and the well‐being of the patients enrolled in one or more clinical trials. The role applies technical and clinical skills to ensure the design of efficient and high‐quality clinical trials, employing quantitative design principles, and clinical best practices to deliver both...
Job SummaryMedpace is currently seeking candidates with PhDs and/or Post-Doctoral Research experience for a full-time, office-based Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team. The aCTM will be a part of the Clinical Trial Management team working with Project Coordinators and Clinical Trial Managers in performance of clinical trial management activities....
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...
Clinical Vendor Manager page is loaded## Clinical Vendor Managerlocations: Milan, Italytime type: Full timeposted on: Posted Todayjob requisition id: R1483993On behalf of our Client a global pharmaceutical company, IQVIA is looking for Vendor Management Lead, Drug Development.The profile will be responsible for selection, contracting, oversight, and performance management of external vendors and...
A leading clinical research organization in Milan is seeking an experienced Clinical Trial Manager to manage day-to-day project operations. This role includes serving as the primary contact for sponsors, developing project plans, and providing oversight of project deliverables. The ideal candidate has over 5 years of experience in clinical trial management, leadership skills, and a passion for...
A clinical research services firm is seeking a Clinical Research Associate in Milan, Italy. This position involves conducting site monitoring visits, ensuring compliance with regulations, and maintaining study documentation. A Bachelor's degree in a scientific discipline or healthcare, along with at least one year of clinical experience, is preferred. The ideal candidate will possess strong...
A leading clinical research firm is seeking an entry-level Clinical Research Associate for their Milan office. This role involves conducting monitoring visits, ensuring compliance with study protocols, and maintaining documentation under supervision. Ideal candidates will have a Bachelor's Degree in a scientific discipline and relevant organizational skills, with proficiency in Microsoft Office....
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...
Clinical Research Associate, Site Management - ItalyEngage in a structured training program to gain knowledge and skills required to independently conduct clinical monitoring visits in accordance with study protocol, standard operating procedures, good clinical practice, and applicable regulatory requirements.Essential FunctionsComplete appropriate therapeutic, protocol and clinical research...
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...