Software Engineering • Senior

Who you are

You have over 2 years of experience in software development, particularly in designing and supporting clinical trial software. Your background includes a strong understanding of programming principles and the ability to develop software components that prioritize patient safety and data integrity. You possess excellent problem-solving skills and are capable of managing your time effectively to meet project deadlines. Your communication skills are strong, allowing you to collaborate effectively with team members and stakeholders.

You are knowledgeable in C#.Net, SQL, and JavaScript, and you understand their related technologies. You have experience in creating technical design and implementation documentation, which helps ensure that all product requirements are met. Your ability to troubleshoot and resolve production issues is a key asset, as you assist the support team in maintaining high-quality software.

What you'll do

As a Senior Software Developer at Suvoda, you will design, develop, and support clinical trial software, focusing on patient safety and the integrity of clinical study data. You will review product requirements to verify that all can be implemented effectively, and assist in creating technical design and implementation documentation. Your role will involve designing and coding software applications, fixing defects, and providing unit testing coverage for the code you deliver.

You will work closely with other team members to ensure timely delivery of high-quality code and manage software deployment into all environments, completing all required documentation. Additionally, you will assist the support team with troubleshooting and resolution of production issues, ensuring that the software operates smoothly and efficiently. Your responsibilities will also include performing other related duties as required, contributing to the overall success of the software engineering team.

What we offer

At Suvoda, we offer a collaborative work environment where you can grow your skills and contribute to meaningful projects in the clinical trial space. You will have the opportunity to work remotely from Romania, allowing for flexibility in your work-life balance. We value our employees and strive to create a supportive culture that encourages professional development and continuous learning. Join us in making a difference in the world of clinical trials and patient safety.