Clinical Research Associate III (CRA, Clinical Monitor): WRAIR CMPNS
Vysnova is currently seeking highly qualified Clinical Reserach Associate III (CRA, Clinical Monitor) for potential full-time work upon award....
Clinical Research Associate I (CRA, Clinical Monitor): WRAIR CMPNS
Vysnova is currently seeking highly qualified Clinical Reserach Associate I (CRA, Clinical Monitor) for potential full-time work upon award....
Primary Purpose The In-House Clinical Research Associate will assist in activities suporting the site management and monitoring of clinical studies, ensuring clinical trials are conducted, recorded,...
Remote WorkPrimary Purpose The In-House Clinical Research Associate will assist in activities suporting the site management and monitoring of clinical studies, ensuring clinical trials are conducted, recorded,...
Remote WorkSenior Clinical Research Associate
Assists with setup, quality and maintenance of the Trial Master Files (TMF) in accordance to Clinical RM SOPs, Good Clinical Practice (GCP), ICH guidelines and federal regulations....
Senior Clinical Research Associate, Internal Medicine, Homebased, US - IQVIA Biotech
Monitors clinical trials in accordance with Good Clinical Practices and procedures set forth by IQVIA Biotech and sponsors....
Clinical Research Associate - General Meds & Oncology
trial reports as assigned Interact with internal work groups to evaluate needs, resources and timelines Act as contact for clinical trial supplies and other suppliers (vendors) as assigned Responsible...
The Research Assistant will develop a progressive functional knowledge of Good Clinical Practices (GCP), Office of Human Research Protections (OHRP) regulations and Food and Drug Administration (FDA...
Responsibilities Submits protocol application and consent forms on behalf of PI to local Institutional Review Board (IRB)....
Remote WorkThe Clinical Research Associate will support the Congressionally Mandated 15-Year study to examine outcome from traumatic brain injury in a military population and the effect on family members....
The Research Assistant will develop a progressive functional knowledge of Good Clinical Practices (GCP), Office of Human Research Protections (OHRP) regulations and Food and Drug Administration (FDA...
Responsibilities Submits protocol application and consent forms on behalf of PI to local Institutional Review Board (IRB)....
Remote WorkClinical Research Associate (Home-base)
Assists with setup, quality and maintenance of the Trial Master Files (TMF) in accordance with ICON Government and Public Health Solutions SOPs, Good Clinical Practice (GCP), ICH guidelines and federal...
Web Announcement Clinical Research Associate The Center for Advancing Correctional Excellence ( ACE!)...
Clinical Research Associate - Field Management - , Va
all monitoring and site management activities....
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Everything we do in healthcare has to be discovered and thoroughly tested before it can be put into practice. In this course, you will explore clinical research its challenges and its huge...
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