Offerte di lavoro clinical study coordinator – Napoli

Provide support to Clinical Affairs team to assure study site selection and conduct of the study by study sites in compliance with Good Clinical Practices, federal regulations, and Clinical Affairs SOPs through in-house and some on-site monitoringConduct pre-study visits to assure the site has adequate facilities, staff, and subject population for conducting...

Overview 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....

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,...

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...

Overview In this role you support regional clinical study delivery to ensure trials run on time, within budget, and to quality standards. You collaborate with the Regional Clinical Study Manager, global teams, and site staff to coordinate feasibility, start-up, TMF, and site communications. You gain hands-on experience in clinical operations and regulatory...

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...

Overview In this role, you will lead site management and monitoring for assigned trials to ensure patient safety and high-quality execution. You will work with cross-functional teams to keep study activities on track from activation to database lock. You will monitor AEs/SAEs and support Drug Safety, audits, and CAPA implementation. This is a remote,...

The successful candidate for this position will be a 1099 contractor with Music Ministry International and be responsible for the following: In accordance with Reference (a), “SECNAV INSTRUCTION 1730.7E,” the Professional Naval Chaplaincy provides for the religious needs and obligations of their people at the very moments and in the very places where...

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 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: R Job Overview Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting...

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,...

About Cogstate At Cogstate, we’re advancing the science of brain health - making it faster, easier, and more accurate to assess cognition across clinical trials, healthcare settings, and everyday life. Our digital cognitive assessments are trusted by researchers, clinicians, and pharmaceutical partners around the world, helping to drive breakthroughs in...

Trial Form Support is seeking a remote oncology clinical monitors to oversee trials across sites, ensuring patient safety, data integrity and regulatory compliance in a fast-paced setting. The role supports study conduct, site management and quality with GCP/ICH adherence, coordinating monitoring activities and audits while enabling meaningful patient...

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...

Senior Study Start-Up Specialist Salary : €53,180 - 82,430 yearly Azienda : Novo Nordisk Tipo Lavoro : Full Time Italy Every clinical trial begins with a critical first step – getting sites ready to enroll patients. In this role, you'll be the driving force behind regulatory and ethics submissions that open the door for breakthrough therapies to reach...

** Please submit your application in English ** What You'll Do: Serve as main CTI contact for assigned study sites Conduct site visits (pre-study (PSV), site initiation (SIV), interim monitoring (IMV), and close-out (COV)) and complete site visit deliverables with quality and within given timelines in Monitoring Plan while adhering to all applicable...

Overview In this role you steer the global clinical development strategy for key respiratory indications, leading a physician-scientist team across geographies. You will align R&D and commercial goals, shape trial designs, and drive regulatory success with high scientific and operational impact. You thrive in a cross-functional, matrix environment and help...

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...

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...

Overview As a Clinical Project Leader, you guide global clinical studies for Parexel’s Large Pharma partners, translating clinical research experience into practical project solutions. You will lead cross-functional teams to deliver trials on time, on budget, and to the highest quality, while ensuring ICH GCP compliance and strong client satisfaction. The...