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Chicago, IL
Research Study Coordinator Responsible for conducting clinical trials according to the protocol, ICH-GCP and other regulatory requirements under the auspices of the PI Collect and complete feasibility...
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3 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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2 days ago
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Jazz Pharmaceuticals Plc
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Philadelphia, PA
monitoring) at clinical study sites to assure adherence to Good Clinical Practices (GCPs), SOPs and study protocols Provide guidance, direction, and management to CRAs Track patient enrollment; qualify...
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2 days ago
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Duke University
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Durham, NC
Develops and submits documentation and information for Institutional Review Board (IRB) review. Communicates with the IRB staff and reviewers and handle issues appropriately....
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2 days ago
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University of California-San Diego
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La Jolla, CA
to the Human Subjects Institutional Review Board (IRB)....
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2 days ago
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Washington University in St. Louis
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Saint Louis, MO
research protocols Performs other duties incidental to the work described herein Required Qualifications: Bachelors degree required; prior work experience, preferably in clinical research support,...
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1 day ago
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Methodist Le Bonheur Healthcare
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Memphis, TN
Clinical Practice guidelines....
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1 day ago
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Cedars-Sinai
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Los Angeles, CA
You will ensure compliance with all federal and local agencies including the Food and Drug Administration (FDA and local Institutional Review Board....
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1 day ago
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Stryker Corporation
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Washington, DC
Proficiency in project management (Microsoft Project or similar software), resource planning, and clinical trial budgeting required. Certified Clinical Research Associate (CCRA) preferred....
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23 hours ago
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Stryker Corporation
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Lansing, MI
Proficiency in project management (Microsoft Project or similar software), resource planning, and clinical trial budgeting required. Certified Clinical Research Associate (CCRA) preferred....
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23 hours ago
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Stryker Corporation
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Atlanta, GA
Proficiency in project management (Microsoft Project or similar software), resource planning, and clinical trial budgeting required. Certified Clinical Research Associate (CCRA) preferred....
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23 hours ago
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Stryker Corporation
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Madison, WI
Proficiency in project management (Microsoft Project or similar software), resource planning, and clinical trial budgeting required. Certified Clinical Research Associate (CCRA) preferred....
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23 hours ago
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Stryker Corporation
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Pierre, SD
Proficiency in project management (Microsoft Project or similar software), resource planning, and clinical trial budgeting required. Certified Clinical Research Associate (CCRA) preferred....
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23 hours ago
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Stryker Corporation
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Santa Fe, NM
Proficiency in project management (Microsoft Project or similar software), resource planning, and clinical trial budgeting required. Certified Clinical Research Associate (CCRA) preferred....
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23 hours ago
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Stryker Corporation
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Saint Paul, MN
Proficiency in project management (Microsoft Project or similar software), resource planning, and clinical trial budgeting required. Certified Clinical Research Associate (CCRA) preferred....
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23 hours ago
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