Under the direction of the Principal Investigator or designee, the Research Coordinator I is responsible for carrying out multiple complex research protocols.

•  Collaborate with investigators in the design, development, and documentation of data forms,       questionnaires, and other survey materials
•  Responsible for aspects of the development of research recommendations and the design of research projects
• Participate in the grant, manuscript, and Institutional Review Board process
• Develop overall research plan for conducting surveys in the community
• Conduct in-person or telephonic field research
• Monitor selection and randomization process of study participants
• Coordinate data collection of study participants, complete case report forms, and develop and maintain spreadsheets
• Collect and maintain questionnaires and other data forms from study participants
• Perform literature searches and write detailed written summaries of the findings
• Collaborate with other project leaders on data presentation, interpretation and writing of scientific reports
• Develop and maintain computerized data files for all data to be collected
• May assist with budget /operational aspect of grant and contract proposals
• Prepare summary reports and ongoing project evaluations for investigators
• May help recruit, select, supervise and direct the activities of data collection employees and Research Technicians
• Conduct quality control check on field data collection system
• Collaborate with other research sites to insure consistency between research sites and accuracy of documentation
• Perform other duties as required.

· Bachelor’s degree in the sciences, health care, or equivalent experience

· 1 year of related experience

· Experience in using computer-based tools (Word, Excel, Access, Outlook, PowerPoint, etc.)

· Oral and written communication skills

· Excellent organization, analytical, and interpersonal skills required

· Ability to travel to off-site locations.

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