Offerte di lavoro per clinical study coordinator in Palermo

IQVIA is seeking a Clinical Study Manager in Italy to provide operational and scientific oversight for assigned trials. The role is full-time and home-based in Italy, with accountability for study delivery at the local level.You will lead clinical teams, coordinate site activation, and ensure compliance with ICH GCP and local regulations. Preferred locations...

Overview In this role you will coordinate the operational management of assigned clinical trials to ensure timely, on-budget delivery compliant with ICH GCP and Chiesi SOPs. You will liaise with multiple stakeholders and manage study budgets and invoicing, contributing to global programs. You will provide operations input during study design, act as a...

Clinical Research Associate I (CRA I) – ItalyLocation: ItalyWorking arrangement: Home-based with travel to clinical trial sitesEmployment type: Full-time, permanentThe OpportunityWe are partnering with an international clinical research organisation seeking a Clinical Research Associate I to support clinical trials across Italy.This opportunity would suit...

Overview In this Clinical Operations Lead role, you will guide strategic and hands-on management of global clinical development programs across Early Phase, Late Phase and RWE studies. You will align cross-functional teams within the Clinical Development Plan and mentor Clinical Project Managers. You’ll oversee end-to-end operations, manage budgets and...

Overview In this role you drive clinical development by supporting global studies and ensuring scientific soundness. You work with cross-functional teams to shape trial design, endpoints and monitoring strategies, while interfacing with health authorities and external experts. You contribute to regulatory documents and publication plans, helping grow our...

Clinical Contracts Associate – Italy Location: Remote, Italy – open to candidates based anywhere in Italy Employment Type: Full-Time, 12-Month Fixed-Term Contract Hours: 40 hours per week Start Date: To be confirmed Project Status: Pipeline opportunity, pending final client approval Client: Leading Global Medical Device Organisation ...

Overview In this role you will lead end-to-end execution of clinical innovation and real-world evidence (RWE) projects within Global Clinical Development. You will collaborate with cross-functional teams to translate strategies into practical plans, ensuring quality, compliance, and timely delivery. The position focuses on secondary data use, RWE,...

Premier Research is looking for a Senior Clinical Research Associate / Clinical Research Associate II to join our Clinical Monitoring, Site Management and SSU team. You will help biotech, medtech, and specialty pharma companies transform life-changing ideas and breakthrough science into new medicines, devices, and diagnostics. What we do is profoundly...

About us Chiesi is an international research-focused biopharmaceutical group with 90 years’ experience, operating in more than 30 countries, with its Headquarter in Parma, Italy. More than 8,000 employees across the group are united by a singular purpose: promoting a healthier world for our people, patients, and the planet. This is what drives us as we...

This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for a Clinical Payments Specialist based in Italy. The Clinical Payments Specialist is responsible for the end-to-end management of global investigator payments across assigned clinical studies. You will oversee payment setup,...

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.We are currently seeking a Senior Clinical Research Associate (CRA) to join our diverse and dynamic...

If you are an experienced Senior CRA who is passionate about oncology research and looking to join a highly skilled and knowledgeable team, TRIO is the place for you! Translational Research in Oncology (TRIO)is a global clinical research organizationdedicated to advancing translational cancer research in the clinical trial setting. Our passionate team is...

Clinical Research Physician, Global Rare Diseases Department: GRD Clinical Development Business Area: R&D, Pharmacovigilance & Regulatory Affairs Job Type: Direct Employee Contract Type: Permanent Location: Europe (flexible) – remote or hybrid What you will do Support the clinical team in relevant medical and scientific aspects of the assigned...

Parexel FSP is hiring for two experienced CRA's at either the CRA II or Senior CRA level to join one of a large Sponsor’s in the EU.This role is responsible for the site management, site monitoring and close-out of assigned clinical trials investigator sites to ensure patient safety and quality study executionSome Specifics About This Advertised RoleEnsure...

Clinical Research Associate, Site Management - Italy page is loaded## Clinical Research Associate, Site Management - Italylocations: Milan, Italy: Milan, Italytime type: Full timeposted on: Posted Todayjob requisition id: R1540967Job Overview Perform monitoring and site management work to ensure that sites are conducting the study(ies) and...

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. As a Study Start Up Associate II at ICON, you will lead the initiation of clinical trials,...

Chiesi Research & Development is seeking an experienced Clinical Operations professional to oversee management of clinical studies from planning through execution. The role requires coordinating CROs, budgets, and timelines while maintaining regulatory standards and project quality.You will contribute to study design discussions, manage risk, and prepare...

Chiesi Global Rare Diseases in Europe seeks a Medical Monitor/Clinical Research Physician to support global clinical studies in rare diseases. You will contribute to study design, risk/benefit assessments, and regulatory document preparation, while ensuring scientific validity and timely publication.Applicants should have a Medical Doctor degree, 2+ years as...

About us Chiesi is an international research-focused biopharmaceutical group with 90 years' experience, operating in more than 30 countries, with its Headquarter in Parma, Italy. More than 8,000 employees across the group are united by a singular purpose: promoting a healthier world for our people, patients, and the planet. This is what drives us as we...

Who we areWe're a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world's most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence. We are Worldwide Clinical Trials, and we are a global team...