17.05.2024 | Full-time | FortreaOf complex clinical regulatory documents including Clinical Study Protocols, Clinical Study Reports, Investigator Brochures, and clinical summary and overview documents in CTD/eCTD format for regulatory submissions world- job is tailor-made for Medical Writers passionate about leading
Uita-te mai târziu17.05.2024 | Full-time | ULAM LABSOperational challenges. Case studyhttps///case-studies/medishout Industry MedTech Technology stack Python, Django - Django Channels, Kubernetes - HELM, React, Azure, Flutter, PostgreSQL Team Poland, 8 people (1x FS Dev & Tech Lead, 1x FE+Mobile Dev, 3x FS Devs, 1x FS - Mobile Dev, 2 QAs
Uita-te mai târziu17.05.2024 | Full-time | ParexelRegion. This person must be fluent in German and main responsibility of the Site Contract Associate is the negotiation of study specific generic and country Clinical Site Agreement (CSA) templates with the Sponsor and support the PL in the negotiation of country budgets with the Sponsor
Uita-te mai târziu16.05.2024 | Full-time | Cluj-Napoca | NATEKIn in Biotechnological sector. Responsibilities Impact Assessment and Configuration changes Analyses - Determine the areas of the system impacted by the study upgrades and define the test scope, scenarios, and test cases accordingly. Analyze the scope of the upgrade and understand the changes made to the system
Uita-te mai târziu16.05.2024 | Full-time | Craiova | HELLAWorldwide and generated consolidated sales of € 6.3 billion in the fiscal year 2021/2022.YOUR TASKSConcept During this program, you will have the opportunity to use theoretical knowledgein practice and you will get the chance to work with the real experts in yourfield of study. It’s a good occasion to get
Uita-te mai târziu16.05.2024 | Full-time | IQVIAActivities in accordance with Study Protocol, Standard Operating Procedures (SOPs), Good Clinical Practice (ICH GCP) and applicable regulatory requirements. Gain an understanding of all aspects of Real-World Late Phase Research, Site Management and Site onsibilities Develop an understanding
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 | 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
Uita-te mai târziu16.05.2024 | Full-time | GfKKickoff 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 suppliers to facilitate communications, trouble-shooting and issue resolution; Coordinate
Uita-te mai târziu16.05.2024 | Full-time | SAPFor real business processes. Your daily tasks will be Study various SAP administration related courses. Work on Technology projects - installation, configuration, upgrade, migration, conversion, greenfield implementation, integration with other systems. Manage customer expectations and avoid escalations
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