Visiting Research Associate II - Department of Medicine, Breathe Chicago Center

University of Illinois • Chicago, IL

395d • $50,000 - $65,000

About The Position

The Visiting Research Associate II at the University of Illinois Chicago's Breathe Chicago Center is responsible for conducting research related to COVID-19 and chronic lung disease. This role involves collecting and documenting study data, ensuring regulatory compliance, and optimizing participant recruitment and engagement. The position may also supervise junior staff and can be performed remotely, focusing on patient engagement via telephone.

Requirements

• Bachelor's degree in social science or related field required.
• A minimum of one year related research experience.
• Knowledge of research concepts, practices, and procedures.

Nice To Haves

• Demonstrated ability to provide customer service involving work with patients, customers, and the general public.
• Proficiency in English and Spanish strongly preferred.
• Experience in a clinical research setting, experience working with federal regulations and IRBs preferred.
• Familiarity with medical terminology and procedures.
• Ability to manage multiple tasks and deadlines.
• Ability to work in a flexible environment with shifting priorities.
• Demonstrated technology skills, including proficiency in Microsoft Office, REDCap, EPIC.
• Excellent written and oral communication skills.

Responsibilities

• Perform surveys, interviews, observations, or use other methods according to established research protocols.
• Collect and review client evaluations/assessments, surveys, and participant interviews to develop reports for the PI and appropriate agencies.
• Assist with study protocol development.
• Maintain compliance with established protocols, regulatory and monitoring agency standards, and grant sponsor guidelines.
• Assess patients for protocol eligibility and participation in clinical research.
• Participate in clinical research education and training programs.
• Execute informed consent process ensuring willingness and understanding of the participant.
• Prepare and contribute statistical data and pertinent information for papers, grants, and other documents.
• Complete required documentation for internal and external regulatory agencies.
• Schedule and conduct clinical research visits required by the protocol and track participant visits.

Benefits

• Competitive salary range of $50,000 to $65,000.
• Comprehensive employee benefits portfolio.

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Industry: Educational Services
• Education Level: Bachelor's degree
• Number of Employees: 10,001+ employees