Job Description We are looking for a highly motivated and experienced Senior Software Engineer, who is very used to working as a key member of a lean, Agile product development team. You will play an essential
Work mode :Remote in Country Onsite Location(s) :Belo Horizonte, MG, SP, BR Additional Location(s) : N/A Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance - At Boston Scientific, we’ll give
The Clinical Systems Specialist is responsible for providing support to internal end users for the Clinical Systems including training, troubleshooting, reporting, and managing user access. More specifically, the Clinical Systems Specialist: - Manage and support the Clinical Systems, including system
The Chief Medical Affairs Office’s Evidence Generation (Ev Gen) Platform is responsible for establishing global scientific leadership and stature through the generation of integrated, end-to-end observational real-world evidence serving all therapeutic areas from proof of concept
The position is for a seasoned individual contributor dedicated to supporting the development, digitization and evolution of an Integrated Evidence Plan, evolving that plan & incorporating into relevant governance documents, and other duties. The Head serve as
responsive, user-friendly front-end interfaces using React with TypeScript. You’ll work closely with your team to ship features that support software solutions in the clinical trial lifecycle, including Electronic Data Capture (EDC) systems and related tools Responsibilities :
The Senior Statistical Programmer will lead single and/or multiple clinical trials and be responsible for the development, maintenance, and validation of annotated Case Report Forms (aCRFs) as well as of specifications and statistical programming of Standard Data Tabulation
The Analytics Center of Excellence Our Analytics Center of Excellence (Analytics COE) harnesses our global healthcare insights, working closely with our clinical and therapeutic experts to power evidence-driven design, speed site activation and recruit the right patients,
The Senior Statistical Programmer will lead single and/or multiple clinical trials and be responsible for the development, maintenance, and validation of annotated Case Report Forms (aCRFs) as well as of specifications and statistical programming of Standard Data Tabulation