I have over five years of experience managing clinical research studies, where I've overseen protocol development, ensured compliance with regulatory requirements, and coordinated between multidisciplinary teams. My role involved patient recruitment, data collection, and analysis, ensuring studies were conducted ethically and efficiently. I've successfully managed studies from inception to publication, contributing to advancements in patient care.

Ensuring compliance involves staying updated with current regulations, such as GCP and HIPAA, and implementing strict protocols for data handling and patient consent. I conduct regular audits, provide team training, and maintain open communication with IRBs. My proactive approach minimizes risks and ensures studies meet all ethical and legal standards, safeguarding participant welfare and data integrity.

One challenging project involved high patient dropout rates. I identified barriers to participation, such as transportation issues, and implemented solutions like remote monitoring and flexible scheduling. By enhancing communication and support, we improved retention. This experience taught me the importance of adaptability and patient-centered approaches in research management.

I prioritize tasks based on deadlines, study phases, and regulatory requirements, using project management tools to track progress. Delegating effectively and maintaining clear communication with my team ensures efficiency. Regular reviews allow me to adjust priorities as needed, ensuring all studies progress smoothly without compromising quality or compliance.

I foster collaboration by encouraging open communication, setting clear goals, and recognizing each member's contributions. Regular meetings and team-building activities strengthen relationships. I also utilize collaborative tools to facilitate information sharing, ensuring everyone is aligned and motivated towards our common research objectives.