• Lead coordination across multiple study sites, including promoting/recruiting research participants and retaining participants in long-term clinical trials. 
• Explain STOP BLOQ study and consent research subjects. 
• Communicate and collaborate with research subjects and site research coordinators to complete data collection.
• Develop and compile data analysis, entry, and management, including analyzing trends and data in recruitment. 
• Assist PI with manuscript writing.
• Assist with coordinating new protocol submissions, renewals, and revisions to Institutional Review Board for multiple studies. 
• Assist PI with manuscript writing and literature searches.
• Participate in the initiation and/or completion of research projects. 
• Record results of experiments: Tabulate research data and keep a detailed, easy to understand laboratory notebook.
• Review progress, troubleshoot, problem solve, and evaluate and interpret experimental research project results.
• Non-scientific lab management as needed; maintain and order supplies, schedule meetings, etc. 
• Day-to-day management of junior lab members and students.
• Train new team members as needed. 
• Work across related clinical projects as directed by PI.
• Attend lab meetings.

Knowledge, Skills, and Abilities:

• Excellent communication skills.
• Great attention to detail.
• Demonstrated ability to manage multiple aspects of complex projects and programs.
• Proficiency in Microsoft products (e.g. Excel®, PowerPoint®, Outlook®).
• Familiarity with using REDCap to build and manage multiple projects.
• Demonstrated ability to work independently.