Job Overview :
Lead EDC RAVE Designer
Remote or Office based EMEA
Lead RAVE Designer required to work for Labcorp Drug Development, one of the largest CROs in the world.
You will be responsible for the development and implementation of solutions to global technical service issues regarding EDC tools like Medidata RAVE.
Office based or home based anywhere in Europe or South Africa.
You must have previous experience of protocol interpretation skills, building databases in the EDC without any specification in place.
Candidates must be fluent in English language (both verbal and written).
In this role, you will build EDC study databases directly from protocol interpretation. You will also create specifications documents to be used for EDC study build and testing.
Join our growing team and discover your extraordinary potential by working as a Labcorp Lead EDC Designer within our Global Clinical Development department.
The position offers a strong support network, flexible working solutions and the opportunity to progress your career. This is a permanent, full-time office or home-based role anywhere within Europe or South Africa.
Job Primary Functions
Development and implementation of solutions to global technical service issues and concerns regarding EDC tools like Medidata RAVE.
Build an EDC study database directly from protocol interpretation.
Create specifications documents to be used for EDC study build and testing.
Manage the EDC study build (and subsequent changes) across multiple teams, including Data Management, Programming, Validation & Testing, and sponsor.
Read, understand and program EDC objects as per the specification documents which meets client requirements and projects.
Perform any post production changes to the EDC database
Reconciliation listings, Protocol Deviations, ACDR listings etc.
Perform publish checks, complex structure dynamics, RSG, Balance mapping settings.
Provide suggestions and solutions to the operational issues. Mentor the team to make them independent enough to perform day to day activities.
Individual Project oversight role.
Project management / oversight across inter and intra teams.
Education / Qualifications :
University / college degree (life science, computer science, programming, pharmacy or related subject preferred), or certification in a related profession from an appropriately accredited institution (e.
g., nursing certification, computer science, medical or laboratory technology).
Good knowledge of drug development process and Clinical Data Management Programming
Good knowledge of relational database
Previous relevant work experience to include data management and database support : EDC systems programming or SAS programming.
Medidata RAVE and protocol interpretation experience strongly preferred
Technical expertise : Design Screens & Program Edits in RAVE
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
Ability to work effectively under minimal supervision
Ability to prioritize work
Ability to mentor and train the team members
Good time management skills and the ability to work to tight deadlines whilst maintain the highest standards of quality work
A cooperative and team oriented approach
Candidates must be fluent in English language (both verbal and written)
NO AGENCIES PLEASE