Bengaluru · Mid Level
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At Clario, a part of Thermo Fisher Scientific, we help the world’s biopharmaceutical companies bring life‑changing therapies to patients faster. Our software platforms support clinical trials across the globe by enabling radiologists, clinical data managers, operations teams, clients, and partners to work with confidence, accuracy, and speed.
We are seeking a Software Engineer with strong experience in C#, .NET, and SQL to join our growing technology team in Bangalore. In this role, you will design, develop, test, and maintain software applications used in regulated clinical trial environments, working closely with cross‑functional stakeholders to deliver high‑quality, compliant solutions.
What We Offer
Competitive compensation aligned with the Bangalore technology market
Comprehensive health and wellness benefits
Paid time off and company holidays
Learning and development opportunities, including technical and regulatory training
A collaborative, inclusive, and purpose‑driven work environment
What You’ll Be Doing
Analyze, design, develop, test, debug, and maintain software enhancements and new applications using C#, .NET, and SQL
Perform requirements analysis and proactively identify gaps, ambiguities, and risks
Clearly distinguish business requirements from technical design and implementation
Follow established development patterns, coding standards, and software lifecycle processes
Write clear, maintainable code with appropriate unit test coverage
Identify, document, and communicate software defects, including steps to reproduce and workarounds
Conduct code and design reviews to identify weaknesses, alternatives, and trade‑offs
Deliver high‑quality, tested code on schedule with a low defect rate
Demonstrate application features and fixes to product management and end users
Partner with Quality Assurance by advising on regression testing focus areas
Troubleshoot production and support issues, isolating defects to specific components
Estimate development effort based on detailed design and contribute to planning activities
Adhere to organizational Standard Operating Procedures (SOPs) and regulatory requirements
What We Look For
Bachelor’s degree strongly preferred
3+ years of professional software development experience
Strong hands‑on experience with C#, .NET, and basic SQL
Experience in clinical trials, life sciences, or pharmaceutical environments preferred
Working knowledge of drug development processes and regulatory requirements, including GxP and 21 CFR Part 11
Proven analytical and problem‑solving skills
Ability to work effectively both independently and in a team environment
Strong written and verbal communication skills
High attention to detail with excellent documentation and organizational abilities
Adaptability to changing priorities and a commitment to quality and service excellence
At Clario, our purpose is to transform lives by unlocking better evidence. It’s a cause that unites and inspires us. It’s why we come to work—and how we empower our people to make a positive impact every day. Whether you’re starting your clinical data career or building long‑term expertise, your work helps bring life‑changing therapies to patients faster.
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