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Aerotek Clinical Research Coordinator in Chicago, Illinois


-Patient Enrolling and consenting (20-30 patients per trial)

-Entering data into various systems

-Following protocol, GCP, ensuing all procedures are meeting requirements

-All phase 1-2 for most part (managing multi site study (sites are all walking distance)

-Monitor and review study performance

-Schedule Patient Visits and meetings with physicians


-A bachelor's degree in a social or health science + 2 years’ experience; or 4 years practical research study or related experience; or a master's degree in a social or health science + 1 year experience is required.

-Cardiology, Neurology, or Oncology experience


Research Project, Clinical Data, Monitoring Tools, Patient recruitment, Oncology, Clinical trial, Clinical research

About Aerotek:

We know that a company's success starts with its employees. We also know that an individual's success starts with the right career opportunity. As a Best of Staffing® Client and Talent leader, Aerotek's people-focused approach yields competitive advantage for our clients and rewarding careers for our contract employees. Since 1983, Aerotek has grown to become a leader in recruiting and staffing services. With more than 250 non-franchised offices, Aerotek's 8,000 internal employees serve more than 300,000 contract employees and 18,000 clients every year. Aerotek is an Allegis Group company, the global leader in talent solutions. Learn more at

The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.