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Online Resumes with "Source Docmentation"
Clinical Research - 10 Years of Experience - Near M1T3N
SUMMARY: * NIH trained Study/Site Coordinator with 10 years of experience in clinical research coordination and administration. * Demonstrated ability in coordinating & implementing Network / Pharmaceutical / Investigator-driven multisite Phase I - IV clinical studies. * Adept in liaising with internal and external stakeholders.
Tags for this Online Resume: Protocol, Clinical Research Associate, Infectious Diseases, ICHGCP, Logistics of study material, Monitoring, Data Entry, Team Lead, Essential Documentation, Informed Consent, SOPs, Coordinator, Regulatory, QA/QC, Source Docmentation, CRF's, TMF, EDC, Toronto, Contracts, SAE
