Research Scientist

• Assist the research coordinator (CRC/CCRC) in conducting clinical trials
• Establish good rapport with potential study subjects
• Collect clinical data, including vital signs, ECG recordings, height, and weight
• Collect and process laboratory specimens as needed
• Schedule study subjects for study visits
• Record and file clinical research data
• Maintain timely records of completed study visits and procedures in the organization’s Clinical Trial Management System
• Review and retrieve medical records

Assistant Research Coordinator

• Aggregate and analyze clinical data and quality reports supporting contract execution and justification
• Aggregate and analyze partnership and programmatic data and quality reports supporting institutional effectiveness and accreditation
• Design study protocols and complete power analyses
• Prepare grants and perform literature reviews
• Develop data extraction forms; extract, manage, and analyze data
• Conduct statistical analyses including descriptive statistics, hypothesis testing, survival analysis, and multivariable modeling
• Provide biostatistical and research-methodology insight and propose statistical approaches for research and quality-improvement efforts
• Disseminate and present scholarly, research, and clinical results
• Report to the Assistant Dean Clinical Affairs
• Perform other duties as assigned