Research Professional 2

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.