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.