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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

Featured Profile

Clinical Research Coordinator

Tags for this Online Resume: Clinical Research Coordinator, Phlebotomist/Lab Tech, Compliance, GCHP, ICH, Research, Clinical Research CoordinatorResearch

Home Based Clinical Research Associate (CRA/Sr CRA) - 20 years experience

I am an RN, certified in clinical research through ACRP. I have 15 years of management experience at a major cancer center and 5 years of clinical monitoring experience both in the field and in-house. For the purpose of clarification, I also have 5 years of clinical research experience as a study coordinator in medicine outside the field of oncology I would like to find a position that matches my level of experience in the...

Tags for this Online Resume: ICH-GCP, Clinical Research Associate, ACRP Certified, Regulatory, Medical Oncology, Medical Device

Quality Assurance Associate Managert

Quality Assurance professional with problem-solving abilities in Pharmaceutical and Biotechnology industries. Primary strengths include US (FDA) 21 CFR, and ICH Q7A Guidance for API Manufacture, Quality Systems development and implementation and strong auditing skills. Introduced and managed electronic document management software including validation, implementation, and maintenance, as well as project team leadership. R...

Tags for this Online Resume: Quality Assurance, FDA regulations, CAPA, Document Control, Change control