Telemedicine Technologies is an engineering company specialising in eHealth information systems, a fast-growing sector with many opportunities.
Telemedicine Technologies’ activity is a mix of various disciplines (Software engineering, space technologies, big data and data science, medicine and clinical operations …) in an international environment and a start-up spirit.
Telemedicine Technologies develops and provides solutions that contribute to improving the care system, patient monitoring and clinical aspects in a wide variety of uses.
You will be part of our software development team or will work on projects for our health sectors clients: pharmaceutical companies, Biotechs, Medtechs, CROs, public hospitals, patient associations…
You could also work on collaborative R&D projects or international programmes
Internship or young graduate, your aim is to obtain new skills, to fully understand the business, the solutions, and Telemedicine Technologies methods. You will also be responsible for: writing software development specifications, developing, testing, validating, configuration and training.
You will be trained in the methodologies, working environment (Hibernate, VAADIN) standards (CDISC), and the quality assurance processes of Telemedicine Technologies Quickly gaining experience, you will use your knowledge and experience to carry out development tasks or increasingly complex project activities.
As a manager you will lead a development team, or you will be in charge of a project to deliver a solution and services that meet all expectations.
A LEADING POSITION AND AN INTERNATIONAL DEPLOYMENT
17-18 Oct 2023 Building on the success of its long-running US-based counterpart, the 6th Annual SCOPE Europe: Summit for Clinical Ops Executives is a two-day executive conference serving clinical innovation leaders, clin ops execs, digital leaders, functional heads, category managers, and those responsible for the planning and management of clinical trials in Europe and the […]
Biopharm International On Sept. 21, 2023, FDA released a new guidance on how the agency plans to utilize alternative tools to remotely evaluate drug manufacturing facilities identified in a marketing application. The application may be a new drug application, an abbreviated new drug application, a biologics license application, or a supplement to any of these […]
Applied Clinical Trials While many US-based biopharma start-ups are interested in conducting clinical trials in Europe, they are often unfamiliar with European legislation and regulations. Some of the biggest misconceptions are around start-up timelines. Typically, the time it takes to go from initial clinical trial application to delivering the first dose to a patient takes […]