You would be working as a Senior Application Specialist on a fixed term contract basis, for client projects in setup, maintenance and decommissioning to ensure delivery of robust, high-quality eCOA solutions using TrialMax platform. On occasion, may be required to support sales efforts. Designs are often complex and may involve multiple company products and computer environments. The role is one that incorporates both Business Analysis - understanding the client's needs, discussing with them its capability, and incorporating the necessary changes. As a Senior Application Specialist, you will be enhancing the tool, using our proprietary language to adapt the tool to provide the information in the way that the client requires, and further developing the tool to ensure the functionality required is in place.
In both our UK and US operations, we would typically have a group of one Senior Application Specialists working in each of our Delivery Teams, you will be working with the Team Manager, the Project Managers and Project Coordinators. A background in SQL and languages such as Java and Python gives you the skills you need to learn our proprietary language. In addition to the pure technical skills you will be learning about our industry and that of our clients, in addition to being a specialist in the CRF Health applications you will soon become an adept Business Analyst with real knowledge of Clinical Trials and Clinical Research.
The Behaviours we will measure you against - the "how you do it" - includes:
Our benefits package includes:
25 days holiday + 8 Public Holidays
Comprehensive Training - starting with a two day "induction" and moving on to further classroom training, self learning and "on the job" training.
Participation in the Company Equity Scheme - you get to own a share in the company
Inclusion in the Company Bonus scheme
Inclusion in the Company Pension Scheme, managed by AXA it includes a company contribution on a matched funds basis.
About CRF Health
Global Leader in eCOA Solutions for Clinical Trials CRF Health is a global leader in eCOA (electronic Clinical Outcome Assessments) solutions for the life sciences industry. eCOA encompasses PROs (Patient Reported Outcomes), ObsROs (Observer Reported Outcomes) and ClinROs (Clinician or Rater Reported Outcomes) with outstanding project management focused on delivering value for our customers. Committed to driving the change to higher quality outcomes and more efficient paper-free clinical trials through improved patient engagement, our intuitive and patient-focused eCOA technology helps companies bring new medicines to market quickly, safely and more cost-effectively. Our complete eCOA solutions are ideal for home and site-based phase I-IV clinical trials across the world for many therapeutic areas and patient populations. More information to be found on our website.
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CRF Health aspires to be the market leading provider of patient centred eSource technology and service solutions focused on flexibility and innovation, underpinned by deep regulatory and technical knowledge and high-quality service delivery.
We have operations in Finland, the US, Romania and the UK and continue to grow in terms of revenues, customer numbers and employees.
CRF Health creates electronic Clinical Outcome Assessment (eCOA) solutions that are simple, scalable, and effective. From our collaborative, agile design approach to our user-friendly reporting tools, we streamline complex processes and deliver reliable results for superior clinical trial outcomes. We improve patient engagement with intuitive design, support study teams with tailored scientific insights, and secure high-quality data with precision. Above all, we ease the path to approval.
Our personalized service and unparalleled eCOA expertise helps sponsors bring new medicine to market quickly and cost-effectively, improving lives across the world. More information on CRF Health to be found at www.crfhealth.com
Details of the benefits offered can be found here.
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The "Behaviours" we will measure you against - the "how you do it" - includes:
How do the decisions in the design and analysis of mode equivalence studies affect study outcomes? Learn more