Integration Configuration Specialist, Iasi, Romania
CRF Health has operations in Finland, the US and the UK with clients based internationally. The company has grown to over 650 permanent personnel (31 March 2018) and continues to grow in terms of revenues, client numbers and employees to support and undertake the work. 2017 has seen the creation of a new office in Iasi Romania which is being populated by R&D, Testing and Operations personnel. We have now grown in Iasi to 95 personnel (April 26th 2018) having only opened the office one year before.
The role of Integration Configuration Specialist will join a team of three people and is key to our continued growth.
Our offices in Iasi are in the Moldova Business Centre, and the sixth floor has recently been refurbished, to our own specification, opened in April 2017
In this role you will work as an Integration Configuration Specialist in client projects including integration between TrialMax system and 3rd party systems like EDC, IRT or Lab systems.
Your main focus is in creating the needed study specific integration configurations for various integration/data transfer protocols including WebServices, REST, FTP etc.
You need to have advanced knowledge of XML and SQL, be able to perform complex queries on the Database and to analyse the results. Deep understanding of XML could be a stepping stone to a career as integration specialist, which means great opportunities and new horizons.
Provides technical integration related support to customers. In addition, contributes also in building the new integration capabilities (adapters) to TIBCO integration platform for new 3rd party systems as needed.
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 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
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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