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Job Description Responsible for performing study site management activities regarding the implementation, monitoring, and summarization of clinical trials to ensure adherence to protocols, Good Clinical Practice (GCP), ICH Guidelines, federal regulations...Yesterday - from: Pharmadiversityjobboard.com
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Job Description Responsible for performing study site management activities regarding the implementation, monitoring, and summarization of clinical trials to ensure adherence to protocols, Good Clinical Practice (GCP), ICH Guidelines, federal regulations...Yesterday - from: Pharmadiversityjobboard.com
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Job Description Responsible for performing study site management activities regarding the implementation, monitoring, and summarization of clinical trials to ensure adherence to protocols, Good Clinical Practice (GCP), ICH Guidelines, federal regulations...Yesterday - from: Pharmadiversityjobboard.com
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Location: Washington, DC
At Kforce Clinical Research, we don't just offer jobs. We offer a rewarding career experience, complete with professional development opportunities and a great benefits package! We are intelligent business partners to some of the world's most valued pharmaceutical...6 days ago - from: jobserve.us -
Salary: Competitive
Location: Virginia - All Locations
Auto req ID 3362BRTitle Regional Clinical Research Associate : Washington DC/VAJob Category ClinicalJob Description Responsible for performing study site management activities regarding the implementation, monitoring, and summarization of clinical trials...4 days ago - from: Tiptopjob.com -
Department: Clinical Affairs
Employment duration: Full time
Lundbeck Inc. (formerly Ovation Pharmaceuticals, Inc.), located in Deerfield, Illinois, was established in March 2009 following the acquisition of Ovation by H. Lundbeck A/S in...7 days ago - from: Campuscareercenter.com -
Job Description Responsible for performing study site management activities regarding the implementation, monitoring, and summarization of clinical trials to ensure adherence to protocols, Good Clinical Practice (GCP), ICH Guidelines, federal regulations...10 days ago - from: Pharmadiversityjobboard.com
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Job Description Responsible for performing study site management activities regarding the implementation, monitoring, and summarization of clinical trials to ensure adherence to protocols, Good Clinical Practice (GCP), ICH Guidelines, federal regulations...10 days ago - from: Pharmadiversityjobboard.com
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Salary: Competitive
Location: Texas - All Locations
Auto req ID 3334BRTitle Regional Clinical Research Associate : Dallas, TXJob Category ClinicalJob Description Responsible for performing study site management activities regarding the implementation, monitoring, and summarization of clinical trials to...11 days ago - from: Tiptopjob.com -
Salary: Competitive
Location: California - All Locations
Auto req ID 3341BRTitle Regional Clinical Research Associate : Los Angeles, CAJob Category ClinicalJob Description Responsible for performing study site management activities regarding the implementation, monitoring, and summarization of clinical trials...11 days ago - from: Tiptopjob.com