Perceptive Informatics is the industry's leading eClinical solutions provider and we help customers accelerate the drug development process through innovation. Our product portfolio is built on leading-edge technology and is combined with extensive medical and clinical expertise. As the technology subsidiary of PAREXEL International Corporation, we're able to leverage our massive investment in technology with our parent company's wealth of hands-on clinical expertise.
As an Associate Software Engineer within Perceptive Informatics, you will be responsible for the delivery and validation of electronic clinical trial management systems. As well as providing technical support to project teams and clients, you be involved in programming, design and development and be capable of bringing 100% customer focus to your work.
Rotational member in any of the Production teams at the direction of the Production Services Management Team
Provide programming skills and expertise in the design and development of bespoke customer projects, change requests, reporting and technical support along with any production development activities
Be responsible for the quality and timeliness of personally assigned workload to agreed timelines, standards and defined requirements. Bringing to the attention of management any circumstances requiring urgent or specific attention at the earliest opportunity
Responsible for all of the unit testing of all code components produced
Work closely with project team members throughout the entire software development life cycle
Provision of technical advice to the internal and external study team, responding to technical queries in good time
Participate in PMD process
Delivering a positive, memorable and meaningful service which exceeds the expectations of both the internal and external customer
Degree or higher degree in Computer Science, Engineering or related discipline
Demonstrable experience of industry standard software development languages and tools such as C#, C++, Java and SQL
Knowledge of relational databases, preferably Oracle
Familiarity with the software development lifecycle and testing methodologies
Ability to prioritize work and meet deadlines
Ability to work and communicate in a project team environment
Ability to interpret and question project requirements documentation
Ability to produce clear and concise technical documentation
Some knowledge of clinical data management process for FDA regulated companies is a plus
Familiarity with FDA regulations such as 21 CFR Part 11 and GxP desirable
In return we will be able to offer you a structured Career Pathway and full training within the role including awareness and understanding of the industry. Your hard work will be rewarded with a competitive salary and benefits package including 25 days holiday per year, pension scheme, tax efficient benefits, health cash plan and other leading edge benefits that you would expect with a company of this type.
reed.co.uk - 9 months ago