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Ascent
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Waltham, MA
Will lead one or more Study Management Teams. Responsibilities: Ensure trial adherence to ICH/GCP/local regulations. Develop study plan(s) including key milestones and timelines....
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2 days ago
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Hackensack Meridian Health
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Neptune, NJ
As the primary resource for the protocols, the CRC will act as liaison between the investigators, primary care providers, the Institutional Review Board (IRB), the Office of Clinical Research (OCR),...
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2 days ago
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Real Staffing
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Boston, MA
Clinical Trial Manager The Clinical Trial Manager will lead the cross-functional team through all activities within the clinical trial life cycle....
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1 day ago
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ICON Clinical Research
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New York, NY
and/or management activities * Previous working experience within the clinical trial management field. * Thorough knowledge of ICH GCP and relevant regulations for the conduct of clinical trials. *...
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1 day ago
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Clinical Research Associates Of Tidewater
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Norfolk, VA
Clinical Research Associates of Tidewater Logo Clinical Research Coordinator Applied 12/02/19 Clinical Research Associates of Tidewater Norfolk, VA Clinical Research Coordinator Clinical Research Associates...
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1 day ago
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ICON Clinical Research
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Houston, TX
and/or management activities * Previous working experience within the clinical trial management field. * Thorough knowledge of ICH GCP and relevant regulations for the conduct of clinical trials. *...
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1 day ago
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ICON Clinical Research
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Newark, DE
and/or management activities * Previous working experience within the clinical trial management field. * Thorough knowledge of ICH GCP and relevant regulations for the conduct of clinical trials. *...
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1 day ago
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ICON Clinical Research
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Gaithersburg, MD
and/or management activities * Previous working experience within the clinical trial management field. * Thorough knowledge of ICH GCP and relevant regulations for the conduct of clinical trials. *...
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1 day ago
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ICON Clinical Research
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Marlborough, MA
and/or management activities * Previous working experience within the clinical trial management field. * Thorough knowledge of ICH GCP and relevant regulations for the conduct of clinical trials. *...
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1 day ago
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ICON Clinical Research
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Philadelphia, PA
and/or management activities * Previous working experience within the clinical trial management field. * Thorough knowledge of ICH GCP and relevant regulations for the conduct of clinical trials. *...
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1 day ago
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Medix
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Palo Alto, CA
database applications Experience with research protocols and regulatory or governing bodies, which include HIPAA and FDA regulations, Institutional Review Board requirements, and Good Clinical Practices...
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1 day ago
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The Ohio State University
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Columbus, OH
to coordinate and perform daily clinical research activities in accordance with approved protocols administered by the non-cancer Clinical Trials Management Organization for the Division of Cardiology...
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1 day ago
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Medix Staffing Solutions
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Cleveland, OH
This candidate will work closely with all research staff to collect, store and maintain data in accordance with FDA Regulations, International Council of Harmonization and Good Clinical Practices....
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1 day ago
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University of Florida
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Gainesville, FL
research trial is maintained and that the trial is conducted in accordance with Good Clinical Practice guidelines; attending UF-IRB 01 full board meetings as necessary. - Miscellaneous Activities Activities...
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1 day ago
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General Dynamics
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Camp Lejeune, NC
The Clinical Research Coordinator is responsible for providing research coordinator support for Institutional Review Board (IRB) approved research protocols....
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2 days ago
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This online course will help you become a more effective clinical supervisor or educator. It is mapped to competences within...
This online course will focus on the principles of workplace-based assessment and commonly used workplace-based...
Imagine a world without research, where governments implement policy based on hunches and manufacturers release products without testing.
Research allows us...
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