11.04.2024 | Pełny etat | Gliwice | Sii Ukraїna TOVThe projects of Sii's key, long-standing client, you will get the chance to develop in the field of R&D, clinical trials, and global services. You will work based on Agile methodologies, using modern tools and technologies. Join our team working on projects of one of the largest pharmaceutical companies
Zobacz później11.04.2024 | Pełny etat | Kraków | Hitachi Vantara CorporationMatter expertise in one or more of the following -medical device QMS -digital patient engagement & experience -clinical & operational analytics -clinical trials software -healthcare data interoperability -remote/continuous patient monitoring with internet of medical things. Experience building systems
Zobacz później11.04.2024 | Pełny etat | Warszawa | Medpace, Inc.Available once eligible. This position plays a key role at Medpace, preparing and reviewing regulatory documents and providing strategic regulatory advice to support clinical trial submissions. Medpace specialises in supporting mid-sized biopharma companies giving you the opportunity to work on complex
Zobacz później11.04.2024 | Pełny etat | Gdańsk (Gdańsk) | FUJIFILM Europe GmbHOverview The primary purpose of the job is to provide general accounting services including supporting the close process through trial balance and reporting on a timely manner and in accordance with quality standards. Responsibilities Processing, execution and compliance of month end activities
Zobacz później11.04.2024 | Pełny etat | VitaliefThe Human Capital epidemic in the Clinical Research Industry and supporting our clients in planning and execution of successful clinical trials. If you are interested in being part of a culture that is highly collaborative, entrepreneurial spirited, have a voice challenging the status quo with novel
Zobacz później11.04.2024 | Pełny etat | Parexel InternationalExperience - all types of visits. Site Management or equivalent experience in clinical research, with understanding of clinical trials methodology and terminology. Ability to perform all clinical monitoring activities independently. Strong interpersonal, written, and verbal communication skills within
Zobacz później11.04.2024 | Pełny etat | Isa Cybersecurity Inc.Our client is one of the leading medical imaging experts on the market. By leveraging their patented cloud-based platform, they assist giant biotech and pharmaceutical companies with drug clinical research and trials. They are a pivotal partner in developing and creating life-changing drugs
Zobacz później11.04.2024 | Pełny etat | Alpine Immune SciencesAre seeking a highly experienced and motivated individual to join our team as the Clinical Supply Chain Director. In this role, you will be responsible for overseeing all aspects of clinical supply chain management to ensure the timely and efficient delivery of investigational drugs for our clinical trials
Zobacz później11.04.2024 | Pełny etat | Warszawa | IQVIA LLCassistant, other medical profession Good knowledge of clinical trials, combined with in-depth knowledge of departmental, protocol and study-specific operating procedures, consent
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