Research Assistant, Data Collection
Overview
Research Assistant will collect and manage clinical data for Metro Infectious Disease Consultants in Chicago. Under Director of Research, you will support multiple research projects, ensuring data accuracy and protocol compliance. This is a 90-day temporary role with potential for extension based on performance. You will work onsite with a M-F (8:30am-5pm) schedule at $20/hour. This role offers direct experience with clinical trial data management and collaboration with Clinical Research Associates.
What You'll Do6
- 1Enter data into the data capture system with high accuracy for sponsor and CRO monitoring.
- 2Maintain organized access to all experimental data for Faculty Researcher and supervisors.
- 3Assist Clinical Research Associates during on-site and remote monitoring visits.
- 4Process invoices for clinical trial budgets and track payments.
- 5Attend project meetings and coordinate with staff via email and phone.
- 6Adapt to evolving project needs and support additional data tasks as assigned.
Requirements4
- 1High school diploma required.
- 2Preferred: completed degree from an accredited institution in social sciences or health-related discipline.
- 3Preferred: experience in the medical field.
- 4Proficiency in Microsoft Office and electronic medical records systems preferred.
Salary Insight
Salary not disclosed in listing
Location
Required Skills
Similar open positions
Explore active roles that match your skills and interests.
Actalent
VerifiedResearch Coordinator Actalent Chicago
Research Coordinator at Actalent in Chicago leads participant recruitment and data management for clinical trials. This role drives efficient study execution while ensuring regulatory compliance and high-quality data handling.
Medix
VerifiedClinical Research Data Assistant Medix
Data Entry Clerk responsible for maintaining accuracy of clinical research data at Medix. Input and verify patient information within electronic systems while ensuring compliance with GCP and HIPAA standards.
107 The Charlotte-Mecklenburg Hospital Authority
VerifiedData Coordinator, Neurosciences Research
You will own statistical data collection and reporting for the Neurosciences Institute, supporting clinical and non-clinical research operations at a major health system. You will compile, analyze, and translate data for management, physicians, and clients, ensuring accuracy and timeliness across monthly and quarterly reports. Working onsite in Charlotte, NC, you will collaborate with research teams and external facilities. This part-time role (12 hours per week) offers a chance to build reporting systems that drive decision making and goal planning in a leading academic medical center.
University of Chicago
VerifiedClinical Research Coordinator 2, Oncology & Multi-Site Trials
You will own the day-to-day execution of 2-5 moderately complex clinical trials, including national and multi-institutional pharmaceutical studies, at the University of Chicago's Department of Surgery. You will work directly with the Principal Investigator and sponsor liaisons, managing subject recruitment, data integrity, and regulatory compliance from start-up to closeout. You will coordinate with a dedicated lab team for specimen processing and ensure protocol adherence across all sites. This role stands out for its depth in GCP and IRB compliance, with opportunities to mentor junior coordinators.
University of Chicago
VerifiedClinical Research Coordinator II at University of Chicago
The Clinical Research Coordinator II leads independent clinical trial activities supporting the Section of Hematology/Oncology at the University of Chicago. This role partners with the Principal Investigator to ensure compliance, financial, and operational integrity across moderately complex studies. Responsibilities span patient recruitment, specimen handling, data management, and regulatory adherence. The position emphasizes autonomy with minimal supervision and offers a competitive salary range of $60,000.00 - $75,000.00.
System One
VerifiedClinical Research Coordinator - System One
Join a busy onsite clinical research site in Dallas, TX as a Clinical Research Coordinator supporting vaccine and other clinical trials. You will coordinate study visits assist with informed consent maintain source documentation and ensure compliance with GCP SOPs. Partner with the PI research staff and participants to drive quality and patient experience.