Senior Technical Designer - Medidata RAVE Certification required

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 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

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](https://himalayas.app/c...