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- Tasks: Lead eCRF design and tackle global technical service issues with Medidata RAVE.
- Company: Join a supportive team in a flexible, home-based role across Europe and South Africa.
- Benefits: Enjoy career progression, a strong support network, and the flexibility of remote work.
- Other info: Dynamic role with opportunities for growth and collaboration in a fast-paced environment.
- Why this job: Make a real impact in clinical data management while working with top sponsors.
- Qualifications: Must be Medidata RAVE certified with experience in specification writing and drug development.
The predicted salary is between 60000 - 80000 £ per year.
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.
Your Responsibilities- 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.
- Conducts 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.
- Good knowledge of drug development process and Clinical Data Management Programming.
- You are Medidata Rave EDC Certified Study Builder.
- You have previous experience of protocol interpretation skills.
Senior Technical Designer - Medidata RAVE certified employer: Fortrea
Contact Detail:
Fortrea Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior Technical Designer - Medidata RAVE certified
✨Tip Number 1
Network like a pro! Reach out to your connections in the industry, especially those who work with Medidata RAVE. A friendly chat can lead to insider info about job openings that aren't even advertised yet.
✨Tip Number 2
Prepare for interviews by brushing up on your eCRF design knowledge and project management skills. We recommend practising common interview questions and scenarios related to your role to show off your expertise.
✨Tip Number 3
Don’t forget to showcase your certification! Make sure to highlight your Medidata RAVE certification during conversations and interviews. It’s a big deal and shows you’re serious about your craft.
✨Tip Number 4
Apply through our website! It’s the best way to ensure your application gets noticed. Plus, we love seeing candidates who take the initiative to connect directly with us.
We think you need these skills to ace Senior Technical Designer - Medidata RAVE certified
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Senior Technical Designer role. Highlight your Medidata RAVE certification and any relevant experience in eCRF design. We want to see how your skills match what we're looking for!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're passionate about this role and how your background makes you a perfect fit. Don’t forget to mention your experience with specification writing and project management.
Showcase Your Attention to Detail: Since attention to detail is key in this role, make sure your application is free from typos and errors. We appreciate candidates who take the time to present their work neatly and professionally.
Apply Through Our Website: We encourage you to apply through our website for a smoother process. It helps us keep track of your application and ensures you don’t miss out on any important updates from us!
How to prepare for a job interview at Fortrea
✨Know Your Medidata RAVE Inside Out
Make sure you brush up on your Medidata RAVE knowledge before the interview. Be prepared to discuss specific features and functionalities of the EDC tool, as well as how you've used it in past projects. This will show that you're not just certified, but also experienced and ready to hit the ground running.
✨Showcase Your Specification Writing Skills
Since the role requires good specification writing experience, come prepared with examples of your previous work. Bring along a few samples or be ready to discuss how you approach writing specifications for eCRFs. This will demonstrate your attention to detail and your understanding of quality standards.
✨Prepare for Client-Facing Scenarios
As this position is client-facing, think about past experiences where you've successfully managed client relationships or led meetings. Be ready to share specific examples that highlight your communication skills and ability to handle project management tasks effectively.
✨Understand the Drug Development Process
Familiarise yourself with the drug development process and Clinical Data Management programming. Being able to discuss how your role as a Senior Technical Designer fits into the bigger picture will impress the interviewers and show that you have a comprehensive understanding of the industry.