Senior Clinical Research Associate- New Jersey
Excellent understanding and working knowledge of clinical research, phases of clinical trials, current International Conference on Harmonization Good Clinical Practice (GCP/ICH) & country clinical research...
Associate Clinical Research (Contract/Full Time/Remote)
The Certified Clinical Research Associate (CCRA) or Society of Clinical Research Associates (SOCRA) credential certification is preferred but not required. + Knowledge of the FDA IDE/PMA regulations...
Remote WorkSenior Clinical Research Associate- New Jersey
in the Clinical Trial Management System, electronic Trial Master File, and various other systems as appropriate and per timelines. + Contributes to Clinical Research Associate team knowledge by acting...
Performs clinical study site management/monitoring activities in compliance with ICH -GCP, Sponsor SOPs, Local Laws & Regulations, Protocol, Si te Monitoring Plan and associated documents....
Clinical Research Associate - Remote (East Coast)
Research Clinical Trials Clinical Works...
Remote WorkTrial Monitoring - Cra/Senior Cra
Implements site management activities to ensure compliance with protocol, GCP, global and local regulations, global and local processes to secure data integrity and patient safety \* Is accountable...
Clinical Research Associate Rutgers, The Of
research related field plus three (3) years of related clinical research experience, two years (2) of which shall have included university level clinical monitoring....
Contract Senior Clinical Research Associate, Oncology Aml
Knowledge of current GCP/ICH guidelines applicable to the conduct of clinical research....
research related field plus three (3) years of related clinical research experience, two years (2) of which shall have included university level clinical monitoring....
Associe principal de recherche clinique / Senior Clinical Research Associate
Excellent understanding and working knowledge of clinical research, phases of clinical trials, current International Conference on Harmonisation Good Clinical Practice guidelines as well as country...
Senior Clinical Research Associate
Performs clinical study site management/monitoring activities in compliance with ICH-GCP, Sponsor SOPs, Local Laws & Regulations, Protocol, Site Monitoring Plan and associated documents....
Performs clinical study site management and monitoring activities in compliance with ICH-GCP, Sponsor SOPs, Local Laws & Regulations, Protocol, Site Monitoring Plan and associated documents....
Associe(e), Recherche clinique / Clinical Research Associate
Performs clinical study site management/monitoring activities in compliance with the International Conference on Harmonisation Good Clinical Practice, Sponsor Standard Operation Procedures, Local Laws...
Associate Clinical Research Medical Director (Remote-US)
Closely collaborate with the Trial Monitoring Organization (TMO) and Medical Affairs to ensure allocation, fast clinical trial start up, recruitment according to planned timelines, early identification...
Remote WorkSenior Clinical Research Associate- Western PA, Ohio
Excellent understanding and working knowledge of clinical research, phases of clinical trials, current International Conference on Harmonization Good Clinical Practice (GCP/ICH) & country clinical research...
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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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