Offerte di lavoro per ich in Palermo

Syneos Health in Italy is seeking a Sponsor Dedicated Senior CRA II – Home Based to oversee clinical monitoring activities across a regional portfolio. You will perform site qualification, initiation, interim monitoring, and close-out visits, either on-site or remotely, ensuring ICH-GCP and GPP compliance and robust data quality.The role requires 6+ years...

Overview In questa posizione, guiderai il controllo qualità in un’azienda chimico-farmaceutica. Lavora a stretto contatto con il responsabile per garantire analisi conformi e affidabili, gestione di convalide ICH e indagini GMP, e supervisione del laboratorio. Offri opportunità di crescita in un contesto di GMP e normativa pharma, con responsabilità di...

Fb Industry Automation entwickelt und realisiert maßgeschneiderte Gesamtlösungen für die Intralogistik. Als Systemintegrator verbinden wir unterschiedliche Technologien zu Lösungen, die auf die Prozesse und Anforderungen unserer Kunden abgestimmt sind. Um unsere Präsenz in Italien weiter auszubauen, suchen wir einen selbstständigen Vertriebspartner,...

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,...

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...

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...

Translational Research in Oncology (TRIO) is seeking a Clinical Research Associate to join the Monitoring Resources team in a home-based role in Italy. The ideal candidate will have at least 2 years of monitoring experience specifically in oncology trials and must be fluent in English. Responsibilities include conducting site visits and ensuring compliance...

Chiesi in Parma seeks a senior leader to drive industrialization and lifecycle management of upstream biopharmaceutical processes. You will lead insourcing, tech transfer, scale‑up, and validation across development to commercial production. The role interfaces with R&D, CDMOs, Production, Quality, and Engineering, applying QbD and ensuring alignment with...

TFS HealthScience is seeking a Freelance Senior Clinical Research Associate (0.4 FTE) to support ophthalmology studies from home in Italy. The role involves on-site or remote monitoring, protocol compliance, and collaboration with sponsors and study teams.The ideal candidate will have 5+ years of independent monitoring experience, GCP/ICH knowledge, and...

IQVIA seeks an Experienced Clinical Research Associate to work from home in Italy. You will perform site monitoring and site management to ensure studies are conducted per protocol, GCP, and ICH guidelines.You will coordinate monitoring visits and ensure timely data reporting to sponsors in a fully remote role. The position emphasizes monitoring activities,...

Overview As a Senior PK Analyst, you will serve as a subject-matter expert within CPMS, delivering PK/PD parameter derivations and supporting data programming for NONMEM, PK/PD datasets, and summary outputs. You work independently on diverse clinical development projects and mentor colleagues. You will apply ICH-GCP standards, drive process improvements, and...

Overview In this Medical Writer role, you support sponsor-aligned clinical development programs by delivering high-quality clinical documents. You collaborate across teams to ensure timely, accurate, and compliant submissions and publications. You will shape documentation strategy and provide lifecycle support from initial drafts to final versions. This...

Overview In this role you will lead and shape the Clinical Project Management function, ensuring compliant, timely delivery of trials across all phases. You will mentor CPMs, optimize resource use, and align project work with portfolio goals. You’ll drive cross-functional collaboration, uphold quality standards, and contribute to strategic planning. This...

Role: Pharmacovigilance Specialist (Remote)Location: Remote (Work from Anywhere)Role Overview:We are hiring for one of our clients, seeking a Pharmacovigilance Expert to work on a full-time basis. This role involves monitoring, evaluating, and reporting adverse events related to pharmaceutical products to ensure patient safety and regulatory compliance. The...

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...

Translational Oncology Research, LLC (TRIO) is seeking a Senior Clinical Research Associate to join our Monitoring Resources team. This full-time, remote position is based in Italy and reports to a CRA Line Manager.You will conduct site visits, ensure FDA/ICH-GCP compliance, manage regulatory documents, and mentor junior CRAs. The ideal candidate has 5+...

Translational Research in Oncology (TRIO) is a global clinical research organization advancing translational cancer research in the clinical trial setting. We are seeking an experienced Clinical Research Associate to join our Monitoring Resources team; this role is home-based in Italy.The CRA will conduct site visits, ensure compliance with FDA, ICH-GCP and...

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...

Responsibilities (a) Site management •     Study site selection, initiation (SIV) and clinical monitoring. •     Perform pre-study visit to ensure eligible sites are selected according to sponsor site selection criteria, including but not limited to adequate resources and experience. •     Prepare and conduct SIV to ensure adequate...

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...