In my previous role, I managed a project involving the coordination of clinical trials across three sites. I prioritized tasks using a Gantt chart, ensuring timely submission of regulatory documents and maintaining clear communication with site coordinators. This experience honed my ability to manage multiple responsibilities efficiently, ensuring all deadlines were met without compromising quality.

I stay updated with current regulations and guidelines by attending training sessions and reviewing industry publications. I also conduct regular audits of processes and documentation to ensure adherence. For example, I implemented a checklist system that reduced errors by 20%, ensuring all procedures met FDA requirements.

I have extensive experience managing clinical data using platforms like Medidata Rave. I ensure data integrity by conducting regular quality checks and resolving discrepancies promptly. In one instance, I streamlined data entry processes, reducing errors and improving overall data accuracy by 15%.

I approach conflicts with empathy and a focus on resolving issues collaboratively. For example, when a team member was struggling with a new protocol, I provided one-on-one training and created a detailed guide to support their understanding. This approach fostered a more cohesive and effective team environment.

I focus on process optimization by identifying bottlenecks and implementing solutions. For instance, I introduced a centralized communication platform that reduced response times by 30%. Additionally, I regularly review workflows to eliminate redundancies, ensuring resources are used effectively.