Offerte di lavoro clinical study coordinator – Genova

Auxologico è alla ricerca di un/a Case Management con gestione e presa in carico dei Pazienti emicranici in concerto con medici ed infermieri nell'ambito del team di ricerca clinica del centro Trial Clinici. Attività e responsabilità: Gestione degli studi clinici interventistici ed osservazionali. Interazione con promotore e direzione scientifica...

As Clinical Research Manager (CRM) in Ophthalmology, you lead clinical operations across multiple studies and countries. You will ensure compliance with ICH-GCP, SOPs, and contracts while partnering with PMs, CRAs, sponsors, and sites. This role focuses on delivering trials on time, in scope, and to high quality, within a global CRO environment. Your work...

Overview Se i requisiti e l'esperienza richiesti per questo lavoro corrispondono alle sue competenze, la preghiamo di candidarsi tempestivamente. As Clinical Research Manager (CRM) in Ophthalmology, you lead clinical operations across multiple studies and countries. You will ensure compliance with ICH-GCP, SOPs, and contracts while partnering with PMs,...

Clinical Research Associate II / Senior Clinical Research (CRA) - ItalyJob Category: Clinical MonitoringRequisition Number: CLINI002065Posted : October 1, 2026Full-TimeRemoteLocationsShowing 1 locationItaly - RemoteDescriptionWhatYou'llDo:Serve as main CTI contact for assigned study sitesConduct site visits (pre-study [PSV], site initiation [SIV], interim...

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...

Trial Form Support is seeking a Clinical Research Manager (CRM) in Ophthalmology to lead clinical operations across studies and countries. You will ensure compliance with ICH-GCP, SOPs, and contracts while partnering with PMs, CRAs, sponsors, and sites in a global CRO environment. The role is home-based with potential in Europe. You will guide CRAs, monitor...

Senior Clinical Research Associate At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON's global expertise. As the world's largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that...

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 timely...

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...

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,...

Trial Form Support seeks a Clinical Research Manager (CRM) in Ophthalmology to lead clinical operations across studies and countries. You will ensure ICH-GCP compliance, SOPs, and contracts while partnering with PMs, CRAs, sponsors, and sites in a global CRO environment. This role offers home-based work in Poland, Spain, or Italy, coordinating with...

Worldwide Clinical Trials is seeking a Senior Clinical Trial Manager for a remote Europe role. You will lead clinical site management from startup through closeout, partnering with project management to drive monitoring strategies and ensure quality and regulatory compliance across oncology studies. You will mentor CRAs and site teams, manage risks, and...

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...

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...

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...