Due to continuous business growth and a strong study pipeline, we are looking for Project Coordinators to join our successful and growing Italian team and engage in clinical trial management on a day to day level. This position will work with our operational teams to accomplish tasks and projects that are instrumental to the company’s success. Responsibilities - Work closely with the Project...
Job Summary :Due to continuous business growth and a strong study pipeline, we are looking for Project Coordinators to join our successful and growing Italian team and engage in clinical trial management on a day to day level. This position will work with our operational teams to accomplish tasks and projects that are instrumental to the company’s success.Responsibilities :- Work closely with the...
Job Overview: Perform 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 Functions: • Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and...
Overview At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You’ll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world. A Day in the Life Study and Scientific Solutions is a global Medtronic team that provides scientific support to all Medtronic Operating Units....
Spécialiste adjoint en recherches cliniques page is loaded## Spécialiste adjoint en recherches cliniquesremote type: Mode de travail Flexible Work Arrangementlocations: Milano, Lombardia, Italytime type: Temps pleinposted on: Offre publiée hiertime left to apply: Date de fin : 1 février 2026 (Il reste 1 jour pour postuler)job requisition id: R58252Chez Medtronic, vous pouvez entamer une longue...
A leading clinical research organization is seeking a Data Manager in Milan, Italy. The role involves acting as the primary communication point for project teams, supervising all data management activities, and coordinating EDC development. Candidates should have at least five years of experience in the CRO industry and proficiency in English. The position promises career advancements in clinical...
JOB SUMMARY Senior Clinical Consultant – Life Sciences (Rif. ANN418147) We are CPL & Taylor by Synergos, an international digital‑solutions consulting firm specialising in the Life Sciences sector. Based in Italy, we support pharmaceutical and biotech companies across regulatory, pharmacovigilance, clinical trials, medical affairs and quality assurance. The role is full‑time, permanent and open...
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...
Company Description PSI 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 Description As aClinical Research Associateat PSI Italy you will enjoy a variety of monitoring...
📌 Location: located in North Italy; Milan 🎯Who 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...
A renowned Contract Research Organization in Milan is seeking a Clinical Trial Assistant to support project execution from start to finish. The ideal candidate will have a Master’s Degree in a scientific discipline or health care, possess strong organizational and decision-making skills, and be fluent in English. This role involves managing study documents, evaluating study sites, and...
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...
A leading clinical research organization in Italy seeks Project Coordinators to manage clinical trials. Responsibilities include working with project teams, maintaining study supplies, and compiling reports. Candidates should have a Master's Degree in Life Sciences and strong communication skills in English. Experience in clinical trials is beneficial. Medpace offers a flexible work environment,...
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....
A global clinical research organization is seeking a Lead Data Manager to oversee data management in complex clinical studies. The ideal candidate will have at least 3 years of experience in data management, proficiency with CDM/EDC systems, and strong organizational skills. Responsibilities include coordinating data activities, ensuring quality control, and communicating with project teams 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...
On behalf of our client, a global pharmaceutical company, IQVIA is looking for a Vendor Management Lead, Drug Development based in Italy. The role is responsible for selection, contracting, oversight, and performance management of external vendors and collaborators supporting clinical development. External vendors include CROs, CMOs, central labs, and bioanalytical labs; external collaborators...
Job Overview Engage in 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 Functions • Complete appropriate therapeutic, protocol and clinical research training to perform job duties. • Gain...
Job Summary Medpace 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....
Job Summary Medpace 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...