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Online Resumes with "clinical regulatory"
Scientist in Regulatory Affairs
Clinical Regulatory Affairs
Clinical Regulatory Affairs - 10 Years of Experience - Near 28201
SUMMARY OF EXPERIENCE: Experienced clinical research professional with more than 15 years in clinical and academic research that has acquired diverse experience in phase II and III clinical drug and device studies with knowledge spanning several therapeutic areas and indications.
Tags for this Online Resume: Protocol, Collection, Documentation, Costing, Consulting, Document Review, Management, Oncology
Clinical Regulatory Affairs
Clinical Regulatory Affairs
Clinical Regulatory Affairs
Clinical Regulatory Affairs
Biological Technician - 13 Years of Experience - Near 60030
Management, regulatory management
Tags for this Online Resume: Administartor, Human Resources, Management, Motorola, Telecommunication, Meetings Organizer, Regulatory Affairs, Arabic Language
Clinical Regulatory Affairs
Experienced and highly qualified Clinical Research Associate with over 10 years of experience in researching and knowledge of study startup, monitoring, and regulatory processes in the Pharmaceutical Industry. Highly proficient in performing quality assurance control on laboratory best practices while leveraging R&D experience to consistently achieve goals. Extremely focused and results-oriented in supporting complex, deadl...
Tags for this Online Resume: Data Management, Documentation, Management, Systems Administrator, Clinical Research, Health Insurance Portability And Accountability Act, Research, Project Management, Project Manager, Protocol
Compliance Officer - 5 Years of Experience - Near 75287
SUMMARY Professional with extensive experience in Regulatory Affairs/Quality Assurance in the medical device, pharmaceutical and automotive industries. Managed and supported domestic and international registrations from new product development, sustaining products to rapid response products. Project Management Market Releases Letters to File International Registrations CN reviews and sign-off Finished good inspections Excel...
Tags for this Online Resume: Assembly Line, Blue Prints, Blueprints, Calipers, CMM (Capability Maturity Model), Product Design, Product Development, Quality, Documentation, Medical
Study Coordinator
Summary Study Coordinator with 6 years' experience specializing in technical support of animal studies requiring GLP compliant interpretations, analysis, documentation, and reporting of results per FDA regulations beginning with protocol development support and creation of shell reports resulting in a Final product ready for FDA Regulatory Filings. Areas of Expertise / Core Competencies * Highly dependable, focused and dete...
Tags for this Online Resume: Documentation, Good Laboratory Practices, Protocol, Analytical Skills, Biomedical Industry, Quality, Quality Assurance, Coordinator, Medical Devices, Regulatory
Quality Manager - 14 Years of Experience - Near 23669
Familiarity with implementation of learning and development practices. ' * Advanced knowledge with quality compliance and regulations. * Phone and in-person consultation with corporate clients. * Attention to detail. * The ability to build and maintain collaborative relationships with customers and coworkers. * Strong work ethic and high standards for performance. * A self-starter that executes with minimal supervision, thr...
Tags for this Online Resume: Compliance, Regulatory Affairs, Inventory, Medical, Medical Devices, Account Management, Accounting, Attention to Detail, Facilitator, Filing, Quality Assurance and Regulatory Affairs