Clin Trials Rsrch Associate - ICTS Clinical Research and Trials Office

• A Bachelor’s degree in a Health Science field or an equivalent combination of education and research experience is required.
• Experience, typically 1-3 years, preparing submissions for institutional review board and other ethical applications.
• Experience, typically 1-3 years, in processing research regulatory documents.
• Working knowledge of Good Clinical Practice (GCP) in research is required. 
• Excellent written and verbal communication skills are required.
• Ability to work flexible hours including nights, evenings and weekends as needed by the research protocol is required.
• Proficiency in Microsoft Word, Outlook and Excel is required.

• Experience with HawkIRB, WIRB, external IRBs, and sIRB submissions.
• Experience with REDCap, Epic and I-CART is desirable.
• Previous experience in data collection and entry is desirable.
• The ability to work independently is desired.
• Excellent time management skills and ability to perform detail-oriented work is desired.

Job openings are posted for a minimum of 14 calendar days. Applications will be accepted until 11:59 PM on February 17, 2020.

Successful candidates will be subject to a criminal background check. Please note regarding references: Five professional references will be requested and required at a later step in the recruitment process.

This position is not eligible for University sponsorship for employment authorization.