In my previous role, I managed a multi-site clinical trial involving 500 participants. I coordinated with various departments to ensure data integrity and compliance with regulatory standards. I implemented a detailed project plan, monitored progress weekly, and addressed any issues promptly. This proactive approach ensured the trial was completed on time and met all objectives.

I prioritize tasks based on deadlines, project milestones, and the impact of delays. I use project management tools to track progress and set clear goals for each team member. Regular team meetings help identify potential bottlenecks and ensure everyone is aligned with the project's objectives.

I implement rigorous training programs for staff to ensure they understand data collection protocols. Regular audits and quality checks are conducted to identify and rectify any discrepancies. Additionally, I use advanced statistical tools to analyze data, ensuring accuracy and reliability.

I address conflicts by fostering open communication and active listening. I encourage team members to express their concerns and work collaboratively to find solutions. For external stakeholders, I maintain transparency and seek mutual understanding to resolve any issues amicably.

I ensure compliance by staying updated with the latest ethical guidelines and regulatory requirements. I conduct regular training sessions for the team and maintain thorough documentation of all research activities. Additionally, I collaborate with the institutional review board to address any ethical concerns promptly.