In a previous role, I managed a Phase III trial with a high dropout rate due to patient discomfort. I implemented a patient engagement strategy, including regular check-ins and personalized care plans, which significantly reduced dropout rates by 20%. This experience taught me the importance of proactive communication and patient-centered care in clinical research.

I meticulously review all study protocols and ensure that every team member is trained in Good Clinical Practice (GCP) and relevant regulations. Regular audits and documentation checks are conducted to maintain compliance. I also stay updated on regulatory changes and adapt our procedures accordingly to avoid any non-compliance issues.

I implement strict data entry protocols, including double data entry and validation checks, to minimize errors. Regular data audits and quality control measures are also part of my routine. Additionally, I ensure that all data management systems are secure and compliant with data protection regulations to maintain data integrity.

I believe in open communication and encourage team members to express their concerns. When conflicts arise, I facilitate discussions to understand all perspectives and mediate a resolution that aligns with the study's objectives. My goal is to foster a collaborative environment where disagreements are seen as opportunities for growth and improvement.

I have extensive experience with various EDC systems, including Medidata Rave and Oracle Clinical. I am proficient in setting up study databases, configuring edit checks, and training staff on EDC usage. My expertise ensures efficient data collection and management, reducing the risk of errors and improving overall study efficiency.