16.05.2024 | Full-time | FortreaAre central to the successful delivery of complex oncology projects for a renowned, innovative and global top pharmaceutical company. Our sponsor is looking for Lead Statistical Programmers capable of overseeing studies from the Pharma side. You will be involved in liaising with the entire study team
Uita-te mai târziu16.05.2024 | Full-time | Cluj-Napoca | AG PrimeRemote and on-site options; Attractive salary and on project bonuses; Possibility to learn advanced software development methodologies; Opportunity for professional development in a young and dynamic environment; Training on the job and possibility to study; Participation in national and international
Uita-te mai târziu16.05.2024 | Full-time | FortreaIn onsibilities includeAll details of site management as prescribed in the project plansRecruitment of potential investigators, preparation of EC submissions, notifications to regulatory authorities, translation of study-related documentation, organization of meetings and other tasksNegotiation of study budgets
Uita-te mai târziu16.05.2024 | Full-time | IQVIAJob OverviewThe medical department consists of a Chief Medical Officer, Medical Directors, medical writers, and safety associates. The Medical Director provides medical and scientific support to clinical research programs, study teams and investigators. The Medical Director also provides review
Uita-te mai târziu16.05.2024 | Full-time | PSIVisitsPerform CRF review, source document verification and query resolutionBe responsible for site communication and managementBe a point of contact for in-house support services and vendorsCommunicate with internal project teams regarding study progressParticipate in feasibility researchSupport regulatory team
Uita-te mai târziu16.05.2024 | Full-time | SySS GmbHOf study, or comparable vocational training You are creative in finding solutions You are an "around-the-corner thinker" You are enthusiastic about operating systems (Linux), networks
Uita-te mai târziu16.05.2024 | Full-time | Cluj-Napoca | WIEGEL Verwaltung GmbH & Co KGAnd training Your profile - committed and independent Completed training or degree in computer science, business informatics or a comparable field of study Good understanding of the relevant business processes in logistics Knowledge of SAP functionalities and customizing of the modules mentioned Technical
Uita-te mai târziu16.05.2024 | Full-time | Parexel& ResponsibilitiesDevelop submission strategies and plans for post-approval CMC activities such as variations, renewals, market expansions, and annual ss change controls and provide regulatory assessments of quality changes in production and quality ew study reports from the quality control
Uita-te mai târziu16.05.2024 | Full-time, Freelancer | IntertekWill be in charge of the following activities· Study both Intertek and Client’s inspection requirements to ensure full understanding before execution· Execute the jobs assigned by manager· Perform inspections, samples collection and other services in accordance with SOP, protocols, respecting the requested timing
Uita-te mai târziu16.05.2024 | Full-time | ProclinicalThe regulatory team in the preparation of study submissions. The successful candidate will also be involved in feasibility research and will be a key liaison for in-house support onsibilities- Direct and report Site Selection Visits (SSV), Site Initiation Visits (SIV), Routine Monitoring Visits
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