Are you an implementation manager or clinical data manager who understands clinical trial data and their data structure, particularly from EDC systems?
We are supporting one of our cutting-edge technology clients in their search for a Risk Based Quality Management Implementation Consultant.

Note this is a permanent full-time position working directly for our client. Their offices are based in Cambridge, however, this can be a fully remote position.  

This is an organisation growing at pace due to the success of their industry leading products and they're looking for an implementation consultant who wants to apply their knowledge and experience to the creation of a leading edge web application for the clinical trials industry.
Ideally you will be excited by the opportunity to have a leading role in the implementation and development of centralized monitoring processes, direct access to the senior leadership team, and the opportunity to be involved in the implementation and continuous development of an application that will truly make a difference to advancements in getting medical treatments to patients.

You will be responsible for:

• Working with the client study teams to define and design Key Risk Indicator (KRIs) and supporting data visualizations
• Working with client data teams
• Creating requirement and technical design specifications that define the data extraction and aggregation routines
• Working with development during the build cycle to ensure the final SQL stored procedures provide the data required for the Study and Site KRIs dashboards, this will include setting up and running SQL queries.
• Reviewing the product study build with the client and accepting the build as complete before handing over to validation
• Delivering to timescales
• Potential to perform periodic centralized monitoring review of the Study and Site dashboards to provide insights in study and site risk profile and recommendations for action depending on requirements and experience 
  
  

This is a great opportunity for someone who is interested in how we can make better use of data in clinical trials to determine which sites, patients and data are most at risk with a view to being able to identify the leading indicators that are predictive of study and site quality. 
While there is a technical component to the build cycle, there is also a great opportunity to gain experience in the practical application of RBQM which requires critical thinking.
 

If this role sounds of interest and you have the relevant skills and experience, please apply today! 

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