In my previous role, I coordinated a multi-site clinical trial involving 150 participants across three states. The challenge was ensuring consistent data collection and adherence to protocols. I managed this by implementing a centralized communication system and regular training sessions for all sites. This approach not only streamlined the process but also improved data integrity and participant engagement.

I prioritize tasks based on their impact on the project timeline and overall objectives. Using tools like Gantt charts and project management software, I allocate resources efficiently and set clear deadlines. Regular team meetings help in adjusting priorities as needed, ensuring that critical milestones are met without compromising the quality of research.

I ensure ethical standards by strictly adhering to institutional guidelines and regulatory requirements. This includes obtaining informed consent, safeguarding participant privacy, and conducting regular ethical reviews. I also foster a culture of transparency and accountability among the research team, which helps in maintaining high ethical standards throughout the study.

I address conflicts by promoting open communication and active listening. I encourage team members to express their concerns and work collaboratively to find solutions. By maintaining a neutral stance and focusing on the project's goals, I help in resolving disagreements amicably and efficiently, ensuring minimal impact on the research outcomes.

To ensure data accuracy, I implement rigorous data collection protocols and regular quality checks. I use validated tools and software for data entry and analysis, and conduct periodic audits to identify and rectify any discrepancies. Additionally, I provide comprehensive training to the data collection team to minimize errors and enhance data integrity.