Software Engineering • Senior

Who you are

You have 5+ years of experience in software development, particularly with .NET technologies. Your expertise in C# and ASP.NET allows you to build reliable and maintainable software systems that prioritize patient safety and data integrity. You understand the complexities of the clinical trial industry and are familiar with the regulations that govern it. You are detail-oriented and can review user requirements specifications to ensure all needs are met within the required timeframe. Your ability to work collaboratively within a cross-functional project team is essential, as you will be developing Interactive Response Technology (IRT) for randomization and drug supply management.

You are skilled in creating implementation design and technical design documentation, ensuring that all aspects of the software development process are well-documented and communicated. Your experience includes managing the deployment of software systems into various environments, completing all necessary documentation to support this process. You are proactive in assisting support teams with troubleshooting and resolving issues reported on production systems, demonstrating your commitment to maintaining high-quality software.

Desirable

Experience with clinical trial technology or a related field is a plus. Familiarity with Agile methodologies and project management tools will enhance your ability to contribute effectively to the team. You are open to learning and adapting to new technologies and processes as needed.

What you'll do

In this role, you will work closely with a cross-functional project team to develop and enhance Interactive Response Technology (IRT) systems. Your primary responsibility will be to ensure that the software meets user requirements and is delivered on time. You will review specifications and collaborate with team members to create implementation and technical design documentation that guides the development process.

You will develop software systems that are not only efficient but also reliable and maintainable, with a strong emphasis on patient safety and the integrity of clinical study data. Your role will involve managing the deployment of IRT systems into all environments, ensuring that all required documentation is completed accurately. You will also assist the support team in troubleshooting and resolving any issues that arise in production systems, contributing to the overall success of the software.

Your work will directly impact the efficiency and effectiveness of clinical trials, as you help shape the digital experiences that enable clinical trial sponsor and site professionals to navigate the complexities of patient interactions. You will be part of a team that is dedicated to improving the clinical trial process through innovative technology solutions.

What we offer

Suvoda offers a collaborative work environment where your contributions will be valued. You will have the opportunity to work on meaningful projects that have a direct impact on patient care and clinical research. We encourage you to apply even if your experience doesn't match every requirement, as we value diverse perspectives and backgrounds. Join us in shaping the future of clinical trials through technology.