27.04.24 | Vollzeit | Marburg | CSL BehringSubmission documents The Role Your main responsibility will be to plan, initiate and perform pharmacology studies, including proof of efficacy, dose range and time course studies within the CV&M Therapeutic Area You will coordinate and report preclinical pharmacological studies (in vivo, ex vivo and in vitro
Später ansehen24.04.24 | Vollzeit | Marburg | CSL BehringTo complex clinical studies. Gathers and documents requirements for clinical supplies based on protocol attributes and clinical assumptions. Influences the protocol design for clinical supply reliability and efficiency. Leads demand forecasting for study(ies); leverages simulation and optimization tools
Später ansehen26.03.24 | Vollzeit | Marburg | CSL BehringOr coding the target solution and preparing the required system design documentation (architectural specifications, diagrams and charts, functional and configuration specifications) to ensure the visualization of the technical implementation of user requirements, and to provide direction to system
Später ansehen26.03.24 | Vollzeit | Marburg | CSL BehringOr coding the target solution and preparing the required system design documentation (architectural specifications, diagrams and charts, functional and configuration specifications) to ensure the visualization of the technical implementation of user requirements, and to provide direction to system
Später ansehen18.03.23 | Teilzeit | Marburg | www.bddh.infoventListener("DOMContentLoaded",function{var e,t,p,a=lementsByClassName("rll-youtube-player");for(t=0;t
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