[Hiring] Senior Technical Designer @Fortrea

Role Description

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 anywhere within Europe in the listed countries and South Africa.

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.

• Development and implementation of solutions to global technical service issues and concerns regarding EDC tool Medidata RAVE
• Responsible for designing the eCRF in leading EDC Rave system
• Responsible for the preparation and/or review draft and final eCRF, edit check specifications for assigned projects to ensure quality and consistency
• Follow attention to detail approach and participate in sponsor meetings and audits/inspections
• Assist Managers in data collection for productivity, quality, timelines, and resource planning
• Responsible for performing quality control procedures for specification development
• Conduct team meetings and provide guidance to Programmers and Data managers
• Participate in the validation of EDC studies when requested
• Responsible for the creation and maintenance of library objects within the Global Libraries
• Responsible for ensuring compliance of standard objects usage throughout the business
• Perform all activities related to specification development for study build and design of databases according to standard procedures

Qualifications

• Good knowledge of drug development process and Clinical Data Management Programming
• Medidata Rave EDC Certified Study Builder
• Previous experience of protocol interpretation skills & building/programming databases in RAVE
• Fluent in English language (both verbal and written)
• Medidata RAVE and protocol interpretation experience strongly preferred
• Technical expertise: Design Screens & Program Edits in RAVE and Inform
• Good problem-solving skills and a proactive approach
• Good oral and written communication skills
• Good knowledge of clinical trial process and data management, biometrics, and systems applications to support operations preferred
• Ability to work in a team environment
• Good time management skills and the ability to work to tight deadlines whilst maintaining the highest standards of quality work
• Minimum 5 years of relevant work experience to include data management and/or database programming and spec design activities

Benefits

• Office 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 company
• Highly competitive compensation packages, including various local benefits such as pension contributions, complimentary health insurance plans, remote working allowances, etc.
• A genuine work-life balance
• Flexibility in working hours
• A thorough onboarding with support from your personal mentor