08.05.2024 | Pełny etat | Wrocław | Mondelez InternationalInformation using modelling and simulation, and pilot plant scale up and factory trials in accordance with good manufacturing practice and HACCP requirements. You will be involved with/lead process design and specifications, process scale-up and commissioning and will ensure the effective use of resources
Zobacz później08.05.2024 | Pełny etat | Parexel InternationalThat the patient is represented at every step 22,000+ employees worldwide 40+ years putting our heart into all we do 1,167 clinical projects in 16 therapeutic areas and 271 indications in 2022 Develop your statistical skills, gain exposure to multiple therapeutic areas, and ecome involved in business development
Zobacz później08.05.2024 | Pełny etat | Warszawa | Precision Medicine GroupOf these life-changing treatments. Precision does this by developing assays that utilize biomarkers to help identify the right patient for the right drug. We handle every aspect of clinical trials from initial strategy and design to selecting sites and executing quality clinical trials. As a Contracts Manager
Zobacz później08.05.2024 | Pełny etat | Gdynia | Frends Technology OyThe trial period. Flat organization structure - you are empowered to do what is needed Lots of possibilities to develop your skills Massages, once a month, held in the office Free car parking Bike parking, shower in the office Relax zone with some fitness equipment in the office Subsidy to private medical
Zobacz później08.05.2024 | Pełny etat | Wrocław | Mondelez InternationalAnd factory trials in accordance with good manufacturing practice and HACCP requirements and development activities (e.g. product shelf-life testing, designing for quality, consumer test preparation etc.). You will also write technical reports that will require the analysis and interpretation of results
Zobacz później08.05.2024 | Pełny etat | Perspective TherapeuticsRequirements, guidelines, and industry trends related to radiopharmaceuticals and cancer therapies, and provide strategic guidance to internal stakeholders. Provide guidance for regulatory aspects of clinical trials, including protocol development, regulatory submissions, and interactions with regulatory
Zobacz później08.05.2024 | Pełny etat | Warszawa | Sportradar Polska Sp. z o.o.Assist in building security practices across one of the most important engineering units in the organization, Enhance security posture across the Engineering unit by implementing security controls based on ISO 27001 standard, Support the establishment of team goals, priorities, KPIs, operating models
Zobacz później07.05.2024 | 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 później07.05.2024 | Pełny etat | ICONFor site negotiation issues and re-pricing for •Observe timelines associated with completion of pricing requests •Build base budget in appropriate systems (ex. eClinical - required in US) Clinical Trial Payment System (CTPS) •Update and review EDC receipts •Create site configuration package for CTPS
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