Clinical Research Assistant (1 year only)
Participates in study-related documentation, such as protocol worksheets, procedural manuals, adverse event reports, institutional review board documents, or progress reports....
Senior Clinical Research Associate - Remote
The Senior Clinical Research Associate plays an integral role in the planning and execution of clinical trials in addition to the management of clinical trial sites to ensure compliance with SOPs, protocols...
Remote WorkSenior Clinical Research Associate
Keywords: Clinical Research, Pharmaceutical, Biotech, Pharma, Global Regulations, Regulatory Compliance, Clinical Study, ICH, GCP, Clinical Trial, Project Management, Regulatory Affairs, Clinical Management...
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...
Clinical Research Associate Institute Of Technology
Specifically, the clinical research associate will assist with data collection, data entry and analysis, dissemination and other general office tasks....
Specifically, the clinical research associate will assist with data collection, data entry and analysis, dissemination and other general office tasks....
Specialist, Clinical Research Monitoring Us Field Mid , Tmtt
form, and determine if clinical trial/study subject documentation is within parameters of study hypothesis, as well as to monitor clinical trial/study safety, in keeping with protocols, GCP (Good Clinical...
Clinical Research Associate - Field Management
all monitoring and site management activities....
Clinical Research Associates Manager
procedures (SOPs), regulations, good clinical practices and study-specific requirements....
Specialist, Clinical Research Monitoring (US Field Midwest Region), TMTT
form, and determine if clinical trial/study subject documentation is within parameters of study hypothesis, as well as to monitor clinical trial/study safety, in keeping with protocols, GCP (Good Clinical...
Specialist, Clinical Research Monitoring (US Field Midwest Region), TMTT
form, and determine if clinical trial/study subject documentation is within parameters of study hypothesis, as well as to monitor clinical trial/study safety, in keeping with protocols, GCP (Good Clinical...
Clinical Research Associate Orthopedics - Research And Development
Certified Clinical Research Professional preferred....
Partnering with clinical trials manager, supports aspects of daily operations within the clinical trials team, including coordinator assignments, trainings, etc....
Lead Clinical Research Associate (Remote) in Chicago, IL
JOB GOAL: Provides administrative and organizational support for assigned clinical trials and sites in accordance with Good Clinical Practice (GCP), guidelines, standards, federal regulations and SOPs...
Remote WorkMoving to Evanston, IL? Find some basic demographic data about Evanston, IL below.
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...
Required or preferred licenses and certifications for Clinical Research Associate positions.
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