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Regional CRA
Aerotek Scientific
- Houston, TX-Managing Institutional Review Board (IRB) and informed consent issues as well as participating in investigator recruitment and site selection visits. -Collecting and verifying...
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Cardiac Research Coordinator - ReqCode 13991
- newBarnabas Health Care Systems
- Newark, NJto the Institutional Review Board (IRB); facilitation of clinical trial agreement execution; assistance with account management of research funds and budget reviews;...
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Consent Form Editor
- newQuorum Review Irb
- WashingtonQuorum Review IRB is looking for a highly detailed-oriented Consent Form Editor. The ideal candidate will evaluate, edit and proofread consent forms and other consent documents...
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Clinical Research Site Manager - CRR-CRSM
Cybercoders
- Sandy, UTClinical Research Site Manager - Clinical Research, Site Manger Clinical Research Site ... to completion and closure - Manages IRB start-up, maintenance and closure...
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Clinical Research Manager Community Specialty Surgical Oncology
Saint Agnes Hospital
- Baltimore, MDBoard. Communicate with the sponsor and IRB for all protocol related issues and SAEs. ... their protocols and ICF and with their IRB submissions. Assist the Principal...
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Clinical Data Manager - Dept of Cardiac/Thoracic Surgery
Penn Medicine
- Philadelphia, PAsupervision by the data manager. The data manager will work closely with the Outcomes ... The Data Manager will also learn from the Outcomes Research Manager how to run queries &...
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Principal Clinical Services Specialist
Valesta
- New Jerseysite budgets, contracts, and also have IRB experience. The employee will have strong computer skills, good organizational skills, ability to prioritize and a good understanding of...
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PROJECT ADMINISTRATOR, Center for Global Health & Development, Grade 73
Boston University
- Boston, MAnagement: Track project "projects" (publications, posters, presentations); maintain project documentation (electronic and hard copy); compile IRB documents Required Skills...
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Clinical Research Associate - R.N.
On Assignment Healthcare Staffing
- Minneapolis, MNincluding documentation of appropriate IRB approvals, negotiation and execution of clinical trial agreements, study personnel authorization documentation, and study personnel...
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Research Coordinator II
University of Massachusetts Medical School
- Waltham, MAof material for project meetings and IRB submissions, summary reports, ongoing ... and termination (includes application for IRB, informed consents, HIPAA Authorization,...
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