Technical Writer - Iasi, Romania
CRF Health is a Software House, developing software solutions used in Clinical Trials. Our product base includes eCOA and Trial Consent. The R&D teams operate out Helsinki, Finland and Iasi, Romania and our customer facing, Technical Services and Delivery Services teams operate out of the UK, the US and from summer 2018, Romania. Our client facing teams comprise of Project Managers, Project Co-Ordinators, Project Assistants, Application Specialists and Associate Application Specialists. Each clinical trial we operate, for our Pharmaceutical clients, require unique tailoring to the tool. The core tool has features including diary reminders and alarms and the scope to capture results from questions written to suit each drugs trial. Our Application Specialists work with the Pharmaceutical companies to ensure that the tool meets the specific needs - creation of alarms and diary reminders, bespoke questions written, so that we can help our clients in understanding patients, volunteers or subjects experience in the drugs trial. Our technical writers are a key component to ensure the user experience. User documentation needs to be created specific to each study. Documentation is written for different groups of people, the clinicians and the subjects. The look and the feel of the documentation needs to be user friendly and we also need the technical writers to be able to take a technical specification and turn it in to language suitable for non-technical people.
We are building the Technical Services and Delivery Services teams. The Technical Writers will work closely with all team members and ultimately will grow to a team of five in Iasi. The first two are being recruited now, with a view to commence work in the summer 2018. During the interview process we will be looking to see examples of your work.
Decision Making and Influence
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. We have recently launched our new Trial Consent solution.
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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