Clin/Tran Research Coord II

Clinical/Translational Research Coord II

1910007

Clin/Tran Research Coord II with Investigating N-3 Fatty Acids to prevent Neonatal Tobacco-related outcomes (INFANTS) Study

The Clin/Tran Research Coord II will support federally funded research projects related to smoking cessation in pregnant women. The Clin/Tran Research Coord II is responsible for coordinating the approval processes and conduct of research proposals, assuring that the integrity and quality of the research is maintained and that the research is conducted in accordance with Good Clinical Practice Guidelines, federal and sponsor regulations and guidelines, Vanderbilt Policy and Procedure and research protocols. Duties include managing screening, implementing recruitment procedures, consent, enrollment, randomization and study conduct from planning through study closeout. The Clin/Tran Research Coord II will manage Clinical Trials Associates. This is a full-time, 40 hour per week, non-exempt term position. The relevant research studies last up to 5 years.

• Prepares and processes new IRB research proposals, amendments, continuing reviews, and adverse event reports

• Prepares and processes information for Clinical Trials.gov

• Assists investigators in implementation, coordination, management and reporting of clinical research operations

• Assist in modification and coordination of research procedures and techniques

• Develop forms and questionnaires for data collection

• Assist in creation of database files and maintain records

• Identifies and procures supplies and equipment needed to fulfill project requirements

• Work with large data sets with attention to detail and accuracy

• Records data from source documentation

• Assist in the preparation of materials for publication

• Read professional journals and attend meetings and/or seminars

• Be knowledgeable of excel data spreadsheets, REDCap, and Access

• Work with all members of the research team in support of additional study-related activities

• Assist the CTA's with subject recruitment, including informed consent

• Other duties as necessary.

• Bachelor's Degree

• 2 years of research experience