Response: Certainly, Avi. One of the major obstacles we encountered during the requirements gathering phase for the clinical trial management system was the complexity of aligning diverse stakeholder needs. The stakeholders included clinical researchers, trial coordinators, and regulatory bodies, each with their own set of priorities and regulatory constraints.

One specific challenge was ensuring that the system could handle the complex data requirements while remaining compliant with stringent regulatory standards. To address this, we conducted a thorough assessment of the existing system and identified critical data points and dependencies that needed to be managed carefully during the migration to the new platform.

We developed a phased migration strategy, which allowed us to transition different components of the platform incrementally. This approach minimized risks and ensured that we could address any issues as they arose without disrupting ongoing operations.

Throughout the process, I worked closely with cross-functional teams, including developers, QA, and compliance experts, to ensure that all requirements were met and that the system was both functional and compliant. Regular communication and iterative feedback loops were key to overcoming these challenges and ensuring the project's success. The project was completed on time, with minimal disruption to the client’s operations, and the new system significantly improved the efficiency of managing clinical trials.