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Metro location, common mid-level software engineer title, and 3+ years requirement increase applicant competition.
Core .NET backend skills transfer across industries, though clinical/regulatory experience is preferred.
Explicit 3+ years plus mandatory C#, .NET, and SQL creates strict technical and experience filters.
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Design, develop, test, and maintain C#/.NET/SQL software applications used in regulated clinical trial environments.
Collaborate with cross-functional teams to deliver compliant, high-quality software solutions on schedule with low defect rates.
Diagnose and troubleshoot production issues, conduct code reviews, and partner with QA to ensure thorough testing and documentation.
Bachelor’s degree strongly preferred.
Minimum 3 years of professional software development experience.
Strong hands-on skills in C#, .NET, and basic SQL required.
Experience in clinical trials, life sciences, or pharmaceutical domains preferred; knowledge of GxP and 21 CFR Part 11 regulations is a plus.
Experienced software engineer with proven ability to deliver compliant software in regulated environments such as clinical trials or pharma.
Detail-oriented with strong analytical and problem-solving skills, capable of writing maintainable, well-tested code following defined processes.
Able to work both independently and collaboratively, with good communication skills and adaptability to changing priorities.