In my previous role, I coordinated a multicenter trial involving 300 participants. The challenge was ensuring consistent data collection across diverse sites. I addressed this by developing a comprehensive training program for site coordinators, conducting regular check-ins, and implementing a standardized data management system. This approach not only streamlined the process but also improved data accuracy and completeness.

Patient safety is paramount. I meticulously review all study protocols to identify potential risks and work closely with the IRB to ensure all ethical guidelines are met. I also provide thorough informed consent processes, regularly monitor participant well-being, and have a robust system for reporting and addressing any adverse events promptly.

Effective budget management involves detailed planning and regular monitoring. I start by creating a realistic budget based on the study's scope and needs. Throughout the project, I track expenses closely, negotiate with vendors for better rates, and adjust the budget as necessary. For timelines, I set clear milestones, monitor progress, and adapt the schedule in response to any delays or changes in project scope.

Conflicts are inevitable in any team setting. I address them by fostering open communication and encouraging team members to express their concerns. I facilitate discussions to understand the root of the issue and guide the team towards a resolution that respects everyone's input. My goal is to maintain a collaborative and respectful environment that aligns with our research objectives.

I have extensive experience with various EHR systems. I utilize them to efficiently extract relevant patient data while ensuring privacy and compliance with HIPAA regulations. I also integrate EHR data with study databases to streamline data collection and analysis, reducing manual entry errors and enhancing data quality for research outcomes.