Associate Software Engineer

Through innovative eClinical solutions and services, Calyx turns the uncertain into the reliable, helping bring new medical treatments to market faster. With deep expertise in clinical development and more than 25 years of supporting trial sponsors and clinical research organizations (CROs), Calyx harnesses that intelligence and activates its potential to solve complex problems, deliver fast insights, and get new drugs to market every day.

Please note: You will be required to work from the Nottingham office fulltime.

Our modern state of the art office in Nottingham city centre has excellent transport links and has a great working environment and the feel of an innovative technology company.

Key responsibilities:

• Rotational member in any of the RTSM 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.

• Cover validation testing as required.

• 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. QualificationsIdeal candidate will possess:

• Degree or higher degree in Computer Science, Engineering or related discipline,

• Or equivalent work experience and have a demonstrable experience and interest in programming using any of the industry standard languages.

• Knowledge of software development languages and tools such as C#, VB.net, 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.