We are currently looking for an experienced Senior Accountant with strong analytical skills and a desire to enhance those skills in a challenging, high visibility environment.
We are currently looking for an experienced Senior Accountant with strong analytical skills and a desire to enhance those skills in a challenging, high visibility environment.
Responsibilities
Sr Bigdata engineer Looking for someone very strong in Scala Programming, python and big data.
Sr Bigdata engineer Looking for someone very strong in Scala Programming, python and big data.
Remote
As a DevOps Engineer, you will be responsible for the planning, design, and implementation of infrastructure for systems such as such as Continuous Integration / Deployment, Source Control, Build Systems, Artifact Repositories and, other miscellaneous systems for production and test environments both physical and cloud. You will plan, build, and implement test automation solutions for medical device software. Through collaboration and frequent interaction with product managers, software developers, and project managers you will create and execute automated test scripts to deploy builds, verify code, and validate correct functionality of the applications. You are self-motivated and like to create new processes and optimize existing ones.
Java Developer using Spring Frameworks with modern software engineering practices and respective tools. Working in a cross-functional agile scrum team, you will be responsible for designing, developing, testing, demoing and documenting enhancements to an enterprise web application
Java Developer using Spring Frameworks with modern software engineering practices and respective tools. Working in a cross-functional agile scrum team, you will be responsible for designing, developing, testing, demoing and documenting enhancements to an enterprise web application
Remote
7+ years of Statistical Programming experience within the life science industry, preferably on the Sponsor side and a relevant BS degree Experience producing TLFs, outputs, reports, and QCing outputs effectively Expertise with SAS statistical software (and other statistical software such as JMP-Clinical, Pinnacle 21, and R) Strong knowledge of CDISC (SDTM & ADaM) Experience supporting regulatory submissions and submissions requirements, relevant ICH and FDA/EMEA/ROW guidelines Experience and understanding of drug development process and clinical trials.
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