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Children's Memorial Hospital
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Chicago, IL
Certification as a Clinical Research Professional (SOCRA) or Clinical Research Coordinator (ACRP) preferred....
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3 days ago
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Merieux NutriSciences Corporation
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Addison, IL
Responsible for ensuring that the clinical trial is conducted according to the investigational plan (protocol) and Good Clinical Practices. Successfully interact with clinical research team....
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4 days ago
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Rush University Medical Center
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Chicago, IL
Clinical Practice (GCP)....
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4 days ago
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IQVIA
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Chicago, IL
of current ICH GCP guidelines and applicable regulations. + Able to mentor CRAs and more junior Clinical Trial Managers. + Able to qualify for a major credit card. + Valid driver's license; ability...
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6 days ago
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Ann And Robert H Lurie
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Chicago, IL
Research Professional (SOCRA) or Clinical Research Coordinator (ACRP) preferred....
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6 days ago
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Ann And Robert H Lurie
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Chicago, IL
Good clinical practices documentation required. 4. Familiarity and experience with FDA and IRB regulatory requirements preferred....
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7 days ago
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Ann And Robert H Lurie
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Chicago, IL
Good clinical practices documentation required.4. Familiarity and experience with FDA and IRB regulatory requirements preferred....
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7 days ago
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Xeris Pharmaceuticals
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Chicago, IL
Collaborate with legal and finance (and others, as needed) on the development and management of study specific agreements (i.e. non-disclosure agreements, clinical trial agreements, clinical research...
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7 days ago
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The University of Chicago
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Chicago, IL
work assignments. 12) Extensive knowledge of Microsoft Word, Excel and Adobe Acrobat. 13) Familiarity with Good Clinical Practices (GCP). 14) Ability to read and understand clinical trials protocols...
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7 days ago
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Randstad Life Sciences
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Deerfield, IL
Comprehensive knowledge and understanding of European/FDA regulations and ICH Guidelines for Good Clinical Practices required....
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10 days ago
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Ann And Robert H Lurie
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Chicago, IL
Certification as a Clinical Research Professional (SOCRA) or Clinical Research Coordinator (ACRP) preferred....
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11 days ago
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The Steely Group
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Oak Brook, IL
While the Principal Investigator is primarily responsible for the overall design, conduct, and management of the clinical trial, the CRC supports, facilitates and coordinates the daily clinical trial...
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12 days ago
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Ann And Robert H Lurie
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Chicago, IL
Certification as a Clinical Research Professional (SOCRA) or Clinical Research Coordinator (ACRP) preferred....
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14 days ago
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Integrated Resources, Inc
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Deerfield, IL
Comprehensive knowledge and understanding of European/FDA regulations and ICH Guidelines for Good Clinical Practices required....
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14 days ago
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Ann And Robert H Lurie
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Chicago, IL
Good clinical practices documentation required. 4. Familiarity and experience with FDA and IRB regulatory requirements preferred....
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15 days ago
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