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Online Resumes with "ICH "
Clinical Research, Research Triangle Park
Savvy, analytical, highly organized and detail oriented individual in search of an interesting position within the realm of clinical trials research. Ideally, the position would allow me to take advantage of my understanding of biology, research methodology, experimental design and medical terminology. I am seeking a position that will lead to a clinical research associate position.
Tags for this Online Resume: Oncology, Clinical Trials, Analytical , Research, GCP/ ICH
Clinical Trials Assistant, RTP
Diligent, accurate and reliable Clinical professional with a reputation for completing high quality, complex diagnostic lab procedures in a timely fashion and in accordance with SOP’s, ICH guidelines and OSHA standards. Eager to learn all broad aspects involving Clinical Research & Development and all scientific and administrartive approaches it entitles.
Clinical Research Professional, Charlotte, ICH/GCP/FDA Trained
Tags for this Online Resume: GCP, ICH, 21 CFR 50, 21 CFR 56, 21 CFR 312, 21 CFR 812, 45 CFR 46, Medical terminology, Data management, Project development, Site monitoring, CRA, CRC
Drug Safety / Pharmacovigilance - RTP, NC
Dynamic, enthusiastic, and performance-driven Doctor of veterinary medicine intent on transferring 10 years of knowledge and experience in a clinical setting to a challenging career working in the Pharmaceutical or Contract Research Organization industry with a progressive company offering opportunities for growth and advancement. Outstanding team player and communicator with highly detailed documentation skills seeking t...
Tags for this Online Resume: Medical terminology, ICH/GCP guidelines, DIsease states, Pharmacology, Customer service, Medical writing
Clinical Research, Raleigh
To Obtain a position congruent with my education and level of experience in the Clinical Research field.
Tags for this Online Resume: Clinical Research Associate, Clinical Research Associate, ICH-GCP Guidelines, ICH-GCP Guidelines, Source Verification, Source Verification, Regulatory Document Maintenance, Regulatory Document Maintenance, Site Initiation Visits, Site Initiation Visits, Drug Accountability, Drug Accountability
Quality and Regulatory Compliance Professional
Certified medical laboratory technologist with extensive experience in pharmaceutical clinical trials, clinical laboratory regulatory compliance, quality assurance, and laboratory management. Experience with most clinical laboratory testing disciplines. Expert instrument troubleshooter and workflow problem solver. Willing to take on challenging situations; attentive to detail; leader, collaborator, or independent worker;...
Clinical Research 14 years experience
My objective is to use my extensive knowledge of clinical research, FDA, ICH, and GCP guidelines to obtain a career in the Pharmaceutical/Biotech industry.
Tags for this Online Resume: Clinical Reserach, IRB, Human Subject Protection, Audit, Monitor
Clinical Project Manager, Sacramento/San Francisco, CA
Tags for this Online Resume: Project Management, Monitor, GCP-ICH, FDA, Clinical Research, Patient Safety, 21 CFR 11, Data Management, Budget and Forecast Planning
