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Offerte di Lavoro Clinical Monitor a Milano
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Risultati di Ricerca - Lavoro Clinical Monitor a Milano
Glenmark Pharmaceuticals-Milano
Pls note: Incumbent can be based anywhere in Europe or the US.
Role Overview:
This position is intended to head and support the clinical development of new drugs conception of innovative approaches to plan clinical studies and support end to end...
IQVIA Italia-Milano
and collaborators based in Italy, supporting clinical development. External vendors include CROs, CMOs, central labs and bioanalytical labs. External collaborators include academic and clinical researchers. This role works cross-functionally with internal...
Glenmark Pharmaceuticals-Milano
support, regulatory presentations and approvals interactions, etc.
• Medical monitoring and supervision of the clinical dermatology studies
• Develops and maintains collaborative partnerships with dermatology stakeholders, key external experts, and allied...
PHIDEALIVE Srl-Milano
Company DescriptionPhidealive Srl is a Contract Research Organization (CRO) based in Milan, Italy, that specializes in Clinical Research services for Pharmaceutical, Biotech Companies, Medical Devices, and Food Supplements. The company operates as...
whatjobs.com -
Barrington James Limited-Milano
Job Description: CNS Clinical Project Manager
Position: Clinical Project Manager – CNS
Location: Milan, Italy
Employment Type: Full-Time
Industry: Biotechnology
Company Overview:
Join a well-established and fully funded biotech company at the...
appcast.io -
OPIS-Monza, 15 km da Milano
The Junior Statistical SAS Programmer, under the supervision of the Direct Manager, is mainly involved in developing SAS programs for the generation of datasets, tables, figures and listings for clinical studies (according to ICH E3), publications...
PHIDEALIVE Srl-Monza, 15 km da Milano
Company Description
Phidealive Srl is a Contract Research Organization (CRO) based in Milan, Italy, that specializes in Clinical Research services for Pharmaceutical, Biotech Companies, Medical Devices, and Food Supplements. The company operates as...
InterSystems Italia-Milano
the trusted expert supporting healthcare organizations in implementing InterSystems solutions effectively and efficiently. Your deep understanding of business processes, clinical workflows, and billing requirements in Italy will be instrumental...
Jefferson Wells Italia-Milano
valuta e seleziona, in collaborazione con il Clinical R&D Manager, con il Clinical Operation Lead ed il Clinical Scientist, i centri sperimentali ed eventuali terze parti, da utilizzare negli studi clinici.
6. Monitora periodicamente il budget di studio...
appcast.io -
Nuraxi.ai-Milano
longevity factors in Sardinia's "Blue Zone" population. You'll contribute to a sophisticated production platform that:
• Processes and visualizes biometric and behavioral data
• Supports clinical trial workflows and health assessments
• Hosts LLM-powered...
Allucent-Milano
Bring your monitoring expertise to the forefront of innovation. We are looking for a Sr. Clinical Research Associate (Sr. CRA) to join our A-team (hybrid). As a Sr. CRA at Allucent, you will independently control and monitor investigational sites...
appcast.io -
Allucent-Milano
Bring your monitoring expertise to the forefront of innovation. We are looking for a Clinical Research Associate (CRA II) to join our A-team. As a CRA II at Allucent, you will independently control and monitor investigational sites, pro-actively...
workable.com -
AppCast-Milano
Company Description
Phidealive Srl is a Contract Research Organization (CRO) based in Milan, Italy, that specializes in Clinical Research services for Pharmaceutical, Biotech Companies, Medical Devices, and Food Supplements. The company operates as...
euspert.com -
Allucent-Milano
Bring your monitoring expertise to the forefront of innovation. We are looking for a Sr. Clinical Research Associate (Sr. CRA) to join our A-team (hybrid). As a Sr. CRA at Allucent, you will independently control and monitor investigational sites...
workable.com -
AppCast-Milano
Participation in the process of collection, classification, data-entry, control, follow up and storage of ICSRs from any source both in the clinical investigation and post marketing settings.
• Participation in the preparation of the safety aggregate reports...
euspert.com -
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