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Senior Technical Designer - Medidata RAVE certified
Fortrea —Maidenhead
- Full-time
- Remote
- English
- Communication skills
- Time management

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Senior Technical Designer - Medidata RAVE certified
Fortrea —Maidenhead
This is a permanent, full-time home-based role anywhere within Europe in the listed countries and South Africa. Good oral and written communication skills.

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Senior Technical Designer - Medidata RAVE certified

Fortrea -
Maidenhead

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Job details

Full-time

Benefits

Company pension

Qualifications

English
Data management
Communication skills
Time management

Full job description

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 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

Your profile:

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 & building/programming databases in RAVE
Candidates must be 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 maintain the highest standards of quality work
Candidates 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 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

Learn more about our EEO & Accommodations request here .

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