Research - Laboratory/Non-Laboratory, Staff/Administrative
The position will coordinate research studies that examine the health effects of tobacco products and e-cigarettes.
Responsibilities: Recruit, consent and run study subjects and process and manage biomarker samples. Prepare and submit regulatory documents (IRB and FDA).
Conduct, coordinate and implement the research study from start-up to closeout according to study protocols.
10% Regulatory activities including IRB applications and FDA correspondence
15% Oversight of site’s study needs in multi-site trial
10% Recruitment, screening, consenting, and enrolling of participants
35% Implementing the protocol for data collection (conducting subject visits, arranging study schedules, coordinating with medical staff)
5% Specimen collection & processing
15% Data entry, data cleaning, and building data reports
5% Survey and form development and management (Qualtrics, REDCap, Word, Excel, Access).
5% Other duties as assigned.
Must be available to work variable hours including some early evening and occasional weekends; time may be negotiable depending on study needs. Must have close attention to detail and able to problem solve. Strong skills in Word, Excel, PowerPoint. Self-starter with strong critical thinking and problem solving skills.
All required qualifications must be documented on application materials.
Bachelor's degree in Psychology, Public Health or related field and at least 2 years of research experience, or a combination of related education and work experience to equal 6 years.
Regulatory experience: IRB application, IND and ITP applications.
Internal Number: 338992
About University of Minnesota, Twin Cities
The University of Minnesota, founded in the belief that all people are enriched by understanding, is dedicated to the advancement of learning and the search for truth; to the sharing of this knowledge through education for a diverse community; and to the application of this knowledge to benefit the people of the state, the nation, and the world.