06.06.2024 | Full-time | GfKTranslation work to align with company quality standards and project budgets;Lead project kickoff meetings for all assigned studies to ensure the all involved parties understand timelines, responsibilities and study specifications;Support research project teams by leveraging relationships with overseas
Uita-te mai târziu06.06.2024 | Full-time | PharmiwebOf clinical trials at a country level in accordance with ICH-GCP and other applicable local regulations. RESPONSIBILITIES OVERVIEW Partner with global, local country teams and study team to provide high level country strategy, drive study progress and country level study delivery. (Accountable for study
Uita-te mai târziu06.06.2024 | Full-time | PwCPreferred Bachelor DegreePreferred Fields of Study English Literature, Journalism, Communications Studies/Speech Communication and RhetoricPreferred Knowledge/Skills Demonstrates
Uita-te mai târziu06.06.2024 | Full-time | PharmiwebIn Romania . Responsibilities include All details of site management as prescribed in the project plans Recruitment of potential investigators, preparation of EC submissions, notifications to regulatory authorities, translation of study-related documentation, organization of meetings and other tasks
Uita-te mai târziu06.06.2024 | Full-time | SAPOn configuring - upgrading - migrating SAP systems used for real business processes. What you'll do Study various SAP administration related courses. Work on platform technology projects - installation, configuration, upgrade, migration, conversion, greenfield implementation, integration with other systems
Uita-te mai târziu06.06.2024 | Full-time | Fruition IT Resources LimitedTo keep developers on the projects until go-live, so this is potentially a project with a lot of longevity that would be a perfect case study for your future CV!The JobAs a Contract Golang Developers you'll have a keen eye for detail, a passion for writing clean, maintainable code, and a strong
Uita-te mai târziu06.06.2024 | Full-time | ProclinicalResolutionCollaborating with experts at study sites and with client representativesQualificationsUniversity degree in scientific discipline or health careAt least 2.5 years of on-site monitoring experienceGood knowledge of clinical research regulatory requirementsVery good computer skills including MS OfficeExcellent
Uita-te mai târziu06.06.2024 | Full-time | IQVIAIQVIA is looking to appoint statistical programmers to utilize the SAS programming language to develop clinical study report materials according to the objectives of a clinical trial for regulatory submissions. Programming and performing related tasks serving the full spectrum of statistical
Uita-te mai târziu06.06.2024 | Full-time | Signant HealthProject Assistant for one of our Global Support Services teams in Iasi working on the Operations area of the business. The position gives you a great view on how a clinical study is being set up. The team is working on managing accesses needed by study personnel once a clinical study is live. Prior
Uita-te mai târziu06.06.2024 | Full-time | Deutsche Rentenversicherung Bayern SüdOthers Release - deployment of the productive applications Participation in the practical training of our junior staff Your profile Successfully completed university degree in computer science or a comparable field of study, alternatively Successfully completed further training in the field
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