26.06.2024 | Full-time | UKSH Gesellschaft für IT Services mbHAt Schleswig-Holstein's largest employer. Our service portfolio includes support for administrative and clinical systems, including customizing applications and providing the IT infrastructure, service desk and IT support. We also provide IT services to UKSH subsidiaries and other external customers. Join our
Uita-te mai târziu26.06.2024 | Full-time | AL SolutionsIn the clinical research industry. They really encourage career progression and prioritise work life balance. Requirements - Life science degree educated - Independent on-site monitoring experience - 3 Years minimum as a CRA - Have in depth GCP knowledge Benefits - Excellent salary and benefits package - Career
Uita-te mai târziu26.06.2024 | Full-time | Arkansas Health ManagementPrograms. Patient Care and Satisfaction Ensure that all patients receive the highest standard of care and customer service. Monitor patient feedback and address concerns or issues promptly to enhance patient satisfaction. Financial Management Implement strategies to maximize clinic profitability
Uita-te mai târziu26.06.2024 | Full-time | Thermo Fisher ScientificOur global Clinical Operations colleagues within our PPD clinical research services provide end-to-end support for clinical trials from study start up to monitoring through to study close out, across commercial and government contracts. Together, we help clients define and develop clinical programs
Uita-te mai târziu26.06.2024 | Full-time | DRV BundIn the area of data protection and IT security of the rehabilitation clinics Monitoring the implementation of measures from the GDPR, the IT baseline protection compendium and accompanying audits in the rehabilitation clinic environment Coordinating the creation and maintenance of cross-departmental concepts
Uita-te mai târziu26.06.2024 | Full-time | Worldwide Clinical TrialsRequisition Number 7966 Position Title Manager, Data Safety & Monitoring Board (DSMB) External Description Who we are Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create
Uita-te mai târziu26.06.2024 | Full-time | Thermo Fisher ScientificOur global Clinical Operations colleagues within our PPD clinical research services provide end-to-end support for clinical trials from study start up to monitoring through to study close out, across commercial and government contracts. Together, we help clients define and develop clinical programs
Uita-te mai târziu25.06.2024 | Full-time | IQVIAParticipants like ECG, BPM, Glucose Monitoring etc. This role will be responsible for business requirement understanding review, test case authoring and UAT executionResponsible for creating site and subject facing documentation like Investigator Manuals, Patient Facing Guides, Site reference guidesResponsible
Uita-te mai târziu25.06.2024 | Full-time | Teva Pharmaceuticalsclinical development and/or post marketing including, as applicable, company sponsored studies, investigator sponsored studies, compassionate use, and disease monitoring programs. Collaborate with other R&D/cross-functional teams to ensure execution of the safety strategy. Contribute to clinical documents
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