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 ResponsibilitiesDevelopment 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 proceduresYour ProfileGood 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 activitiesWhat You Can Expect From UsOffice based or home based anywhere in Europe or South Africa (listed countries)Rewarding and meaningful work in an established, diverse, highly profitable and respected global companyHighly competitive compensation packages, including various local benefits such as pension contributions, complimentary health insurance plans, remote working allowances etc.A genuine work life balanceFlexibility in working hoursA thorough onboarding with support from your personal mentor Fortrea is actively seeking motivated problem-solvers and creative thinkers who share our passion for overcoming barriers in clinical trials. Our unwavering commitment is to revolutionize the development process, ensuring the swift delivery of life-changing ideas and therapies to patients in need. Join our exceptional team and embrace a collaborative workspace where personal growth is nurtured, enabling you to make a meaningful global impact. For more information about Fortrea, visit www.fortrea.com.Fortrea Is Proud To Be An Equal Opportunity EmployerAs an EOE/AA employer, Fortrea strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, colour, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. We encourage all to apply.For more information about how we collect and store your personal data, please see our Privacy Statement.If, As a Result Of a Disability, You Require a Reasonable Accommodation To Complete Your Job Application, Pre-employment Testing, Job Interview Or To Otherwise Participate In The Hiring Process, Please [email protected]. Please note that this e-mail address is only for job seekers requesting an accommodation. Please do not use this e-mail to check the status of your application.Learn more about our EEO & Accommodations request here. Show more Show less