Clinical Data Manager & Study Coordinator (Clinical Trial)
Istituti Clinici Scientifici Maugeri
L’Istituto Clinico Scientifico Maugeri cerca un Clinical Data Manager/Study Coordinator per gestire i dati clinici di uno studio prospettico. Interverrai in collaborazione con i team di ricerca interdisciplinari, assicurando integrità e coerenza dei dati.
Competenze in e-CRF e gestione database, con incarico della durata di 12 mesi in regime co.co.co. Verrà valorizzata l’esperienza e le conoscenze linguistiche. La sede è a Pavia.
#J-18808-LjbffrOfferta di lavoro pubblicata 1 giorno fa
Offerte di lavoro simili
- ph3Clinical Data Manager/Study Coordinator-Progetto di ricerca /h3 pLa figura selezionata svolgerà... ...e gestione dei dati clinici relativi al clinical trial prospettico in oggetto, in collaborazione... ...liPartecipazione a incontri di coordinamento/aggiornamento in presenza o...Consigliato
- ...medical leadership for clinical trials and serve as the... ...expert for study reports and regulatory... ...a chance to shape trial strategy and execution... ...Provide medical management and expertise for... ...manuscripts Manage safety issues in trials and coordinate evaluation with team...ConsigliatoLavoro ibridoLavoro da casaOrario flessibile
- ...medical oversight for clinical trials and serve as the... ...monitor for sponsor-led studies. You act as the... ...safety monitoring, data review, and cross-functional... ...and safety data; coordinate with Safety Management Oversee data... ...consensus ~ Capacity to manage multiple projects...ConsigliatoLavoro da casaTurni
- ...Overview In this role you will oversee clinical trial activities to ensure protocol alignment, regulatory compliance, and data integrity. You will monitor sites, conduct... ...regulatory knowledge Proven ability to manage multiple sites and projects simultaneously...Consigliato
- ...will lead site management and monitoring for assigned trials to ensure patient... ...teams to keep study activities on... ...to meaningful clinical development across... ...Manage site-level activities... ...compliance Coordinate information flow... ...knowledge of clinical trial methodologies,...ConsigliatoRemoto
- ...Overview In this role you oversee clinical trial monitoring to ensure adherence to protocol... ...patients faster by maintaining rigorous data integrity and site performance. You will... ...regulatory requirements Proven ability to manage multiple sites and projects...
- ...you will support multinational clinical studies by coordinating site activities and ensuring high-quality data. You will work within a cross... ...team to monitor sites, manage regulatory submissions, and help... ...You'll contribute to compliant trial conduct aligned with GCP and...Auto aziendaleOrario flessibile
- ...contribute to designing and analyzing clinical trials, ensuring data quality and patient safety while... ...resolve data queries, and prepare key study documents. This role sits at the heart... ...medicines, offering opportunities to impact trial conduct and regulatory compliance....
- ...role you steer the global clinical development strategy... ...commercial goals, shape trial designs, and drive... ...trials Ensure optimal study designs, endpoints, and... ...influencing at senior levels Data interrogation and... ...planning and program management Regulatory submission...RemotoOrario flessibile
- ...medical leadership for clinical trials, guiding scientific strategy, trial execution, and reporting... ...internal medical expert for study results interpretation... ...-functional teams to manage safety, regulatory documents... ...and sponsor meetings Coordinate with other departments...Lavoro ibridoOrario flessibile
- ...this role you lead end-to-end data management delivery for single or multi-... ...offers influence over study validation, data integrity, and... ...procedures within a data-driven clinical research environment. Responsabilità... ...and client expectations Manage service levels and timelines...
- ...this role you join Medpace's Clinical Monitoring team in Italy to... ...investigator qualifications, manage data integrity, and support site... ...to drive successful clinical trials. Travel up to 60-80%... ...Communicate with site staff including coordinators and investigators to ensure...Orario flessibile
- ...contribuendo a realizzare valore tramite modelli operativi di Data Governance e misurazione degli esiti. Unisci competenze tecniche... ...sintesi per guidare cambiamenti organizzativi e tecnologici nel data management. Responsabilità Analizzare obiettivi di business,...
- ...Programming (DBP) team and shape the clinical database to capture study data from paper and electronic CRFs.... ...success. Responsabilità Lead and coordinate the DBP team to meet project... ...systems Strong knowledge of Data Management processes and pharma guidelines (...
- ...this role you coordinate the operational management of assigned clinical projects to... ...stakeholders, ensuring study quality,... ...of clinical data. This... ...Responsabilità Manage 1–3 clinical trials depending on... ...for ongoing studies Requisiti... ...Clinical trial management and...Remoto
- ...strategic delivery of global clinical trials, partnering with... ...guide multi-regional studies, ensuring quality, timelines... ...Drive proactive risk management, issue resolution, and... ...knowledge of clinical trial conduct, ICH-GCP, and... ...relationships and manage senior stakeholders...
- ...In this role you will coordinate the operational management of assigned clinical trials to ensure timely, on-budget... ...stakeholders and manage study budgets and invoicing,... ...computation and control for studies/programs Support... ...~ Clinical trial planning and design...Remoto
- ...Overview In this role you will manage day-to-day clinical trial operations and serve as the primary sponsor... ..., and contribute to protocol and study deliverables. This position sits in Medpace... ...on protocol, edit check specs, and data analysis plans Develop operational...Orario flessibile
- ...Overview In this Clinical Trial Manager role, you will oversee day-to-day trial... ...compliance and delivery of study milestones. You will act as... ...area knowledge to manage risks, vendors, and site quality... ...protocol, edit check specs, data analysis plan, and final report...RemotoOrario flessibile
- ...Overview As an Associate Clinical Trial Manager at Medpace, you join... ...with project coordinators, clinical trial managers... ...work on coordinating study timelines, quality... ...third-party vendors Manage and perform quality control... ...project timelines Coordinate project meetings and...Orario flessibile
- .../ppbr/ppbSenior Medical Science Liaison Manager (F/M/X) Italy /b /ppbr/ppOur client is a... ...relationships with KOLs, HCPs, academic centers and clinical study sites /pp✅ Lead peer-to-peer scientific... ...and communicate relevant clinical data /pp✅ Support congresses, advisory boards...Lavoro da casa
- ...As Project Manager at Alira Health... ...execution of study protocols within... ...partner with the Clinical team, sponsors... ...to keep trials on track and deliver... ...Manage clinical studies to meet scope,... ...supply, IWRS/IXRS, data management, biostatistics... ...to achieve trial milestones...
- ...based role you join the Clinical Trial Management team as an aCTM,... ...collaborate with Project Coordinators and Clinical Trial Managers to deliver study activities with high... ...-party vendors Manage and perform quality control... ...project timelines Coordinate project meetings and...Tempo pienoOrario flessibile
- ...role you support multicenter clinical studies by monitoring sites to ensure protocol adherence and data reporting per GCP/ICH guidelines... ...to project needs, and manage study progress and documentation... ...support start-up Maintain Trial Master File and Investigator's...
- ...role you join Medpace's Clinical Monitoring team in... ...activities for clinical studies. You will receive comprehensive... ...to ensure quality data and patient safety,... ...with site staff, coordinators and clinical research... ...regulatory document review Manage regulatory documents...RemotoLavoro da casaOrario flessibile
- ...Medpace you will support the integrity of clinical studies across pharmaceutical and medical... ...functional teams to ensure compliant trials and data quality, with substantial travel.... ...Communicate with site staff including coordinators and physicians Verify investigator...Orario flessibile
- ...you join Medpace's Clinical Monitoring team to support site-based trials in Italy, helping advance... ...and contribute to data integrity and site... ...directly impact trial quality, patient safety, and timely study delivery.... ...approved protocol Coordinate with site staff including...Tempo pienoOrario flessibile
- ...leadership forums, governance committees, and executive routines with strong preparation and follow-up Support the T&S Governance Manager in defining and evolving the T&S Strategy Create executive presentations, dashboards, and communications for the T&S Leadership...Lavoro ibrido
- ...definire e governare l'architettura dati end-to-end in un contesto internazionale orientato all'innovazione digitale. Layer di decisione data-driven con responsabilità di evoluzione della piattaforma dati e roadmap tecnologica. Avrai responsabilità operative su data...
- ...patient outcomes. You'll drive real-world and clinical research efforts and lead high-integrity... ...programs and investigator-sponsored studies Lead scientific communication,... ...~ Strategic mindset with stakeholder management and communication skills ~ Ability to...