What You’ll Be Doing
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Design and contribute to both logical and low-level solution architecture.
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Develop high-quality source code based on detailed specifications, delivered on time.
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Perform thorough unit testing and document outcomes in alignment with test plans and quality standards.
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Participate in reviews of functional specifications and provide implementation support.
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Collaborate with Senior Software Engineers to review, refine, and standardize code for quality and consistency.
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Troubleshoot and resolve technical issues during solution deployment.
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Ensure documentation accuracy and support quality assurance through regular code and test coverage reviews.
What We Look For
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Bachelor’s degree in IT, computer science, engineering, or a related field (or equivalent experience)
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Minimum of 3 years in software development, ideally within a product lifecycle environment in a regulated or healthcare setting
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Strong programming skills in Java, Python, C#, .NET Framework
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Familiarity with XML standards / HTML, UML 2.0, and Enterprise Architect (Sparx Systems)
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Unix Knowledge
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Experience with MS SQL Server (2005/2008R2+), IIS, and Visual Studio®/Team Foundation Server.
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Proficiency with Microsoft Windows operating systems and Office applications
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Solid understanding of object-oriented programming, software design patterns, and risk management techniques
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Experience in GMP documentation and working within Clario’s quality management system (Nice to have)
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Knowledge of clinical trial technology and regulated software development
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Fluent in English, with strong written and verbal communication skills
What we Offer
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Competitive compensation
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Medical, dental, and vision insurance (starting Day 1)
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Flexible work schedules
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Flex PTO plan
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Remote and hybrid work options
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Engaging employee programs
EEO Statement
Clario is an equal opportunity employer. Clario evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status, or any other legally protected characteristic.
The duties and responsibilities listed in this job description represent the major responsibilities of the position. Other duties and responsibilities may be assigned, as required. Clario reserves the right to amend or change this job description to meet the needs of Clario. This job description and any attachments do not constitute or represent a contract. The Department Head has the discretion to hire personnel with a combination of experience and education, which may vary from the above listed qualifications.
Top Skills
What We Do
-- Clario has been named a Top Workplace by Energage for the 2022 Top Workplaces USA national awards. --
Clario generates the richest clinical evidence by fusing our deep scientific expertise and global scale into the broadest endpoint technology platform. By doing this, we empower our partners to transform lives.
With almost 50 years of experience, 19,000 clinical trials, and 870 regulatory approvals, Clario has mastered the ability to generate rich evidence across a Trial Anywhere™ portfolio: decentralized (DCT), hybrid and site-based clinical trials. With 30 facilities in nine countries across North America, Europe, and Asia Pacific, Clario delivers the power of certainty.
Partners
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Clario brings the best of ERT and Bioclinica together to
work alongside our partners to solve some of their biggest questions on topics such as:
- eCOA vs. paper
- Decentralized Clinical Trial (DCT)
- Rescue a clinical trial
- Broad endpoint technology: cardiac safety, imaging, respiratory
And many more.
People
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We are so honoured to be named a 2022 Top Workplace by Energage. One of our leading values at Clario is People First Always. We help individuals build meaningful careers at Clario as they serve to help transform patients lives.
Join us on this journey and check out our careers page:
https://clario.com/careers/
