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Online Resumes with "GCP FDA guidelines"
Senior Clinical Research Coordinator
To obtain stable, long-term position in the industry where my experience and skills will be an asset
Ideal Companies: Pharmaceutical, Medical device, Hospital/clinics, Government
Tags for this Online Resume: Senior Clinical Research Coordinator, Clinical Research Monitor-Medical Devices, Study Manager-start up CRO, Regulatory Affairs Specialist, IRB Coordinator/Specialist, Mental Health Counseling-College Graduate, GCP, ICH
Clinical Research - 7 Years of Experience - Near 10803
Qualification Highly motivated and accomplished Clinical Research Coordinator with extensive skills and experience. Nine years of experience as an Oncology research coordinator. Proven ability to manage multiple studies simultaneously. Managed phase 1b - IV protocols according to GCP and FDA guidelines. Experience as a supervisor and mentor to study coordinators across various oncology disease sites. Trained staff on study ...
Tags for this Online Resume: Appraisals, Audit, Clinical Research, Data Quality, Documentation, Management, Protocol, Quality, Quality Assurance, Recruiting
Admissions Director - 0 Years of Experience
SUMMARY * Pharmacovigilance Associate with over 2+ years of experience in Drug Safety and Clinical practice fields with clear understanding of EDC (Electronic Data Capture) * Experience in performing successful data management, triage, case entry, MedDRA, WHOdrug dictionaries, narrative writing, peer review, case follow-up, case review and report preparation * Performing Data entry and Quality check adverse event reports fr...
Tags for this Online Resume: Quality, General Practice, HYGIENE, Medical, Surgical, Acceptance Testing, Assessments, Business Intelligence, Coding, Database, healthcare