Senior Technical Designer – Medidata RAVE Certification Required

🔥 15 hours ago

🌐 United Kingdom, Romania, +3 more countries – Remote

🇬🇧 United Kingdom – Remote 🇷🇴 Romania – Remote 🇧🇬 Bulgaria – Remote 🇵🇱 Poland – Remote 🇭🇺 Hungary – Remote

⏰ Full Time

🟠 Senior

✍️ Designer

👻 Ghost score 10%

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Fortrea

WebsiteLinkedInAll Job Openings

10,000+ employees

🏥 Healthcare

🧬 Biotechnology

💊 Pharmaceuticals

Healthcare • Biotechnology • Pharmaceuticals

Fortrea is a global clinical research organization (CRO) specializing in providing comprehensive clinical development services to biopharma and MedTech companies. With over 30 years of experience, Fortrea offers a range of services including clinical pharmacology, phase I-IV study management, regulatory strategy, market access, and more. They focus on advancing healthcare innovation by integrating data and scientific expertise to deliver tailored solutions that enable faster decision-making and improve patient outcomes, especially in the realm of cell and gene therapy programs, as well as various therapeutic areas like oncology, cardiovascular, and infectious diseases.

📋 Description

• Develop and implement solutions to global technical service issues and concerns regarding Medidata RAVE EDC • Design eCRFs in the leading EDC Rave system • Prepare and/or review draft and final eCRF and edit check specifications for assigned projects • Participate in sponsor meetings and audits/inspections • Assist Managers with data collection for productivity, quality, timelines, and resource planning • Perform quality control procedures for specification development • Conduct team meetings and provide guidance to Programmers and Data Managers • Participate in EDC study validation when requested • Create and maintain library objects within Global Libraries • Ensure compliance with standard object usage throughout the business • Perform specification development for study build and database design according to standard procedures • Lead eCRF design within assigned projects in a client-facing, project-management-focused role

🎯 Requirements

• Medidata Rave EDC Certified Study Builder certification • Previous experience with protocol interpretation and building/programming databases in RAVE • Fluency in English, both verbal and written • Technical expertise designing screens and programming edits in RAVE and Inform • Good knowledge of drug development processes and Clinical Data Management Programming • Good problem-solving skills and a proactive approach • Good oral and written communication skills • Good knowledge of clinical trial processes and data management, biometrics, and systems applications to support operations preferred • Ability to work in a team environment • Good time management skills and ability to work to tight deadlines while maintaining high quality standards • Minimum 5 years of relevant work experience, including data management and/or database programming and specification design activities • Medidata RAVE and protocol interpretation experience strongly preferred

🏖️ Benefits

• Strong support network • Flexible working solutions • Opportunity to progress your career • Competitive compensation packages • Pension contributions • Complimentary health insurance plans • Remote working allowances • Genuine work life balance • Flexibility in working hours • Thorough onboarding with support from a personal mentor