Required:

• Excellent skills in computer and software operation 
• Knowledge of health services or clinical research methodology and principles.
• Prior IRB experience and coordination of clinical studies desired.
• Experience following strict research imaging protocols and data entry
• Knowledge and experience using word processing, spreadsheet, and statistical software programs (preferably Microsoft Word/Excel/Publisher/Access)

Preferred:

• Previous experience in data management of clinical research protocols, including the completion of case report forms and other study documents. 
• Prior IRB experience and coordination of clinical studies desired.
• Excellent writing skills, as evidenced by co-authorship or authorship of research or technical reports, in order to write or edit correspondence, progress reports, and research papers 
• Experience administering structured questionnaires
• Knowledge of basic statistical tests and procedures related to data management and selection of descriptive tests for summarizing data.
• Experience tracking subjects and managing follow up assessments
• Knowledge or experience in working with large animals
• California phlebotomy certification, ACRP or SoCRA (or equivalent certification).
• RN Licensure, BS, MS, or other degree, or several years' professional research or analytical experience.
•  Attentive to detail and have knowledge of cross-sectional anatomy and medical terminology.
• Knowledge of simple statistical analysis.