In my previous role, I managed multiple IRB submissions, ensuring all protocols adhered to federal and institutional guidelines. I prepared detailed documentation, including consent forms and study protocols, and maintained open communication with the IRB to address any concerns. My proactive approach minimized delays, and I consistently met submission deadlines. I also conducted regular audits to ensure ongoing compliance, staying updated on regulatory changes to implement necessary adjustments. This experience has equipped me with a strong understanding of ethical research practices and the ability to navigate complex regulatory landscapes effectively.

I employ a strategic approach to recruitment, leveraging diverse channels such as community outreach, social media, and partnerships with healthcare providers. I ensure clear communication about study goals and benefits to potential participants, addressing concerns to build trust. For retention, I maintain regular contact, provide reminders, and offer incentives when appropriate. I also prioritize participant comfort and convenience, scheduling visits at flexible times. By fostering positive relationships and demonstrating respect for participants' time and contributions, I have consistently achieved high recruitment and retention rates in my previous studies.

I implement rigorous data management protocols, including double-data entry, regular audits, and validation checks to ensure accuracy. I train study staff on proper data collection techniques and provide detailed guidelines to minimize errors. Additionally, I use secure electronic data capture systems to maintain data integrity and prevent unauthorized access. Regular monitoring and cross-checking of data against source documents help identify and correct discrepancies promptly. My systematic approach ensures high-quality data, which is critical for reliable research outcomes and regulatory compliance.

I prioritize tasks based on urgency and impact, using project management tools to track progress and deadlines. I break down larger projects into manageable steps and delegate tasks when appropriate, ensuring team members are aligned with goals. Regular check-ins help me stay on top of timelines and address potential bottlenecks early. I also maintain open communication with stakeholders to manage expectations and adjust priorities as needed. My ability to stay organized and adaptable has allowed me to successfully manage multiple studies simultaneously without compromising quality or compliance.

In one study, a participant expressed discomfort with a specific procedure. I immediately paused the process and consulted the study protocol and IRB guidelines to explore alternatives. I worked with the research team to modify the procedure, ensuring it still met study objectives while respecting the participant's concerns. I documented the incident and reported it to the IRB as required. By prioritizing the participant's well-being and adhering to ethical standards, I maintained trust and ensured the study's integrity. This experience reinforced the importance of flexibility and ethical decision-making in human subject research.