Seeking to utilize my professional expertise in a clinical trial setting supporting good clinical practices as a clinical research associate. I am motivated to promote my efficient skills in being a quick learner, multi-tasker, detail oriented, proactive, and having great organization and communication skills. I uphold high quality standards and able to respond to rapidly changing priorities.
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clinical , research , medical , monitoring, devices, CRF
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Clinical Research, IRB Submissions, Federal Regulations, Good Clinical Practices, Protocol Analysis, Data Collection , Regulatory Coordination
Based on my extensive experience in a variety of Health care and Clinical Research companies, I am confident that I would be a great asset to any organization.
My expertise includes quality review of documents, processes and systems, root cause analysis, and CAPA investigation. In addition, my projects have focused on the development of the internal/external audits and risk assessments, audits of final clinical reports, po...
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Quality Assurance, Clinical Research, Pharmaceutical, Blood Banking, GCP, ICH
Ideal Companies: MedImmune, NIH, Social & Scientific Systems
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triage, clnical trials, auditing, informed consents, study protocols, communications
I know biology. I know bioethics. I know good clinical practices. Now, I want to do them.
Ideal Companies: University of Chicago, Northwestern University, University of Illinois at Chicago, Rush University
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Research, Clinical, Data
High energy with interperonal, communication and leadership skills. Resourceful and very responsible
Ideal Companies: Laboratory, enviromental, Public Health, Customer Service
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research assistant, administrative assistant, customer services, research technician, case manager
My goal is to continue to grow and establish myself as a Clinical Research Associate.
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data management, standard operating procedures, good clinical practice, attention to detail
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GCP Auditor, Clinical Auditor, GLP Auditor, Quality Assurance, Clinical Trails, Good clinical practice