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Merck Company
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Fort Lauderdale, FL
Performs clinical study site management/monitoring activities in compliance with International Council for Harmonisation Good Clinical Practice (ICH-GCP), Sponsor Standard Operating Procedures (SOPs...
Remote Work
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1 day ago
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Merck Company
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Atlanta, GA
Performs clinical study site management/monitoring activities in compliance with International Council for Harmonisation Good Clinical Practice (ICH-GCP), Sponsor Standard Operating Procedures (SOPs...
Remote Work
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1 day ago
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Merck Company
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Kenilworth, NJ
Excellent understanding and working knowledge of clinical research, phases of clinical trials, current GCP/ICH & country clinical research law & guidelines....
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1 day ago
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Medtronic Inc.
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Phoenix, AZ
Ability to manage multiple clinical research sites with proven results in study execution. Experience in Good Clinical Practice (GCP) and/or regulatory compliance guidelines for clinical studies....
Remote Work
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2 days ago
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Medtronic Inc.
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California, MD
Ability to manage multiple clinical research sites with proven results in study execution. Experience in Good Clinical Practice (GCP) and/or regulatory compliance guidelines for clinical studies....
Remote Work
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2 days ago
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Medtronic Inc.
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New Haven, CT
Ability to manage multiple clinical research sites with proven results in study execution. Experience in Good Clinical Practice (GCP) and/or regulatory compliance guidelines for clinical studies....
Remote Work
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2 days ago
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PPD
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Wilmington, NC
Clinical Trial Management System)....
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2 days ago
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Covance
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Raleigh, NC
Experience: A minimum of at least 9 months of Onsite Clinical Monitoring experience and 2 years total in clinical research experience is required....
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1 day ago
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Seattle Children's
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Seattle, WA
Seattle Childrens Clinical Research Associate I Apply Now Seattle, WA External Description We have an opening for a Clinical Research Associate I to join the team!...
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1 day ago
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South Shore Hospital
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Weymouth, MA
The CRA will work with the Principal Investigator(s) to ensure Institutional Review Board (IRB) requirements are met....
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1 day ago
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Inspire Medical Systems Inc
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Minneapolis, MN
data collection and good clinical practices * Communicate directly with clinical centers to maximize enrollment, ensure quality and timely data capture and answer study-related questions * Perform...
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6 hours ago
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Parexel
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Waltham, MA
Trial Management System (CTMS), Electronic Document Management System (EDMS) and MS-Office products such as Excel and Word.A little about us Parexel is proud to be a leading Clinical Research Organization...
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5 hours ago
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Covance
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San Antonio, TX
Experience: A minimum of at least 9 months of Onsite Clinical Monitoring experience and 2 years total in clinical research experience is required....
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1 day ago
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Covance
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New Orleans, LA
Experience: A minimum of at least 9 months of Onsite Clinical Monitoring experience and 2 years total in clinical research experience is required....
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1 day ago
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Covance
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Dallas, TX
Experience: A minimum of at least 9 months of Onsite Clinical Monitoring experience and 2 years total in clinical research experience is required....
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1 day ago
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