Are you a SQL programmer, clinical data manager or study implementation consultant, who loves building innovative systems, looking for a move into technology? Our client has a great industry leading product and is looking to expand their team so this is an exciting time to join them too. 

We've got a great Risk Based Quality Management Implementation Consultant (Data Manager) role. This role is client facing so you will need to have good communication skills. This is a remote position but our client's offices are in Cambridge. 

Our client is growing at pace due to the success of their Industry leading products. We are 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. We can consider a range of skills for this role, so if you want to be a subject matter expert/ technical expert or mentor and manage teams, there may be these opportunities too. 

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. 

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