Offerte di lavoro clinical study coordinator – Firenze

TFS HealthScience is seeking a Project Management Associate to join the study team and provide administrative support to the Project Manager within the assigned therapeutic unit. You will help plan, set up, execute, and close‐out clinical studies, maintain study documents and CTMS records, coordinate meetings, and assist with vendor management, payments,...

Clinical Research Associate II / Senior Clinical Research (CRA) - Italy Job Category : Clinical Monitoring Requisition Number : CLINI Posted : October 1, 2026 Full-Time Remote Locations Showing 1 location Italy - RemoteDescription WhatYou'llDo: Serve as main CTI contact for assigned study sites Conduct site visits (pre-study (PSV), site initiation (SIV),...

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...

Are you being referred to one of our roles by a connection in Alira Health? If so, please apply using the referral link emailed to you. Join our global team dedicated to innovation and initiative, where physical walls and different time zones don't limit, but encourage, collaboration. Where all contributions and new ideas are explored with an open mind and...

Overview In this home-based role, you will monitor clinical trials in oncology across sites, ensuring patient safety, data integrity, and regulatory compliance. You'll work within the Strategic Resourcing Solutions team to support study conduct, site management, and quality by adhering to GCP/ICH and SOPs. You'll coordinate monitoring activities, manage...

Why Join Clinical Functional Service Partnerships (CFSP)? At IQVIA, our Clinical Functional Service Partnership (CFSP) models offer the best of both worlds: the opportunity to work as an integrated member of a leading sponsor's team while benefiting from the global expertise, career development and support of IQVIA. CFSP roles provide the opportunity to...

CTI is seeking a Clinical Research Associate II / Senior CRA to support sites in Italy, focusing on regulatory compliance and timely deliverables. You will act as the main CTI contact for assigned sites and manage site visits throughout pre-study through close-out phases. The role requires 3–5 years of CRA experience with a strong life-science background,...

Who We Are We’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. Who We Are We’re a global, midsize CRO that pushes...

Clinical Independent Rater - Romanian Speaking Location: Remote/Virtual Hours: Estimated 10–16 hours per month Role: Clinical Independent Rater for Clinical Trials About IQVIA IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services, dedicated to driving healthcare forward. We partner with the world’s leading...

Trial Form Support is seeking a remote Clinical Monitor to oversee oncology trials across sites, ensuring patient safety, data integrity, and regulatory compliance. You will coordinate monitoring activities, manage documentation, and participate in audits while supporting study conduct within a global, collaborative team. The role requires a Bachelor's in...

This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for a Clinical Site Payment Associate Manager based in Italy. As a Clinical Site Payment Associate Manager, you will play a key role in managing clinical trial site payments, ensuring financial accuracy, regulatory compliance, and...

Overview In this role you coordinate the operational management of assigned clinical projects to advance Chiesi’s pipeline in line with medical standards. You act as the primary liaison to CROs, providers, and internal stakeholders, ensuring study quality, timelines, and budget adherence. You play a key part in study design input and risk management,...

Who we are We'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...

Who we are We’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...

In this role, you contribute to the design and analysis of clinical trials within ICON's sponsor-dedicated model. You will monitor sites, ensure protocol adherence, data integrity, and patient safety, and collaborate with investigators to ensure smooth study conduct. You'll review data, resolve queries, and help prepare study documents to support trial...

Pharma D&S cerca un/una Clinical Trial Assistant con almeno 1 anno di esperienza maturata come CTA o Study Coordinator nel contesto della Ricerca Clinica. La risorsa supporterà il Project Manager nelle impostazioni dello studio, assisterà nella presentazione del pacchetto di documenti regolatori agli enti etici e alle autorità regolatorie...

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...

Organisation/Company Università LUM Research Field Medical sciences » Medicine Researcher Profile Recognised Researcher (R2) Leading Researcher (R4) First Stage Researcher (R1) Established Researcher (R3) Application Deadline 9 Oct 2026 - 12:00 (UTC) Country Italy Type of Contract To be defined Job Status Not Applicable Is the job funded through the EU...

General Description: The CRA executes clinical monitoring activities at clinical trial sites and monitors clinical trials in accordance with ICH guidelines and GCP, local regulations, and applicable SOPs. Performs monitoring activities related to selection, initiation, conduct (recruitment, quality data collection) and timely completion of...

TFSHealthScience is seeking an experienced Clinical Research Manager (CRM) to join our Ophthalmology team. This home-based role is open to candidates located in Poland, Spain, or Italy, including Italy’s Lazio/Roma area. You will coordinate country- and site-management activities, ensure compliance with ICH‑GCP and regulatory requirements, and drive...