Senior Technical Designer - Medidata RAVE Certification required

Senior Technical Designer – Medidata RAVE certified  Join our growing team and discover your extraordinary potential by working as a Senior Technical Designer within our division, working with some of our most important sponsors.  The position offers a strong support network, flexible working solutions and the opportunity to progress your career.  This is a permanent, full-time home-based role in the United Kingdom, Romania, Bulgaria, Poland, Czech Republic, Hungary. In a client-facing and project management focused role, you will lead eCRF design within the scope of assigned projects. We are looking for an experienced and certified RAVE database designer who has good specification writing experience.   Your responsibilities: Development and implementation of solutions to global technical service issues and concerns regarding EDC tool Medidata RAVEResponsible for designing the eCRF in leading EDC Rave systemResponsible for the preparation and /or review draft and final eCRF, edit check specifications for assigned projects to ensure quality and consistencyFollow attention to detail approach and participate in sponsor meetings and audits/inspectionsAssist Managers in data collection for productivity, Quality, timelines and resource planningResponsible for performing quality control procedures for specification developmentConducts team meetings and provide guidance to Programmers and Data managersParticipate in the validation of EDC studies when requestedResponsible for the creation and maintenance of library objects within the Global LibrariesResponsible for ensuring compliance of standard objects usage throughout the businessPerform all activities related to specification development for study build and design of databases according to Standard procedures Your profile: Good knowledge of drug development process and Clinical Data Management ProgrammingYou are Medidata Rave EDC Certified Study BuilderYou have previous experience of protocol interpretation skills & building/programming databases in RAVECandidates must be fluent in English language (both verbal and written)Medidata RAVE and protocol interpretation experience strongly preferredTechnical expertise: Design Screens & Program Edits in RAVE and InformGood problem solving skills and a proactive approachGood oral and written communication skillsGood knowledge of clinical trial process and data management, biometrics, and systems applications to support operations preferredAbility to work in a team environmentGood time management skills and the ability to work to tight deadlines whilst maintain the highest standards of quality workCandidates must be fluent in English language (both verbal and written).Minimum 5 years of relevant work experience to include data management and/or database programming and spec design activities   What you can expect from us:Office based or home based anywhere in Europe or South ...