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Online Resumes with "ICH GCP "
Scientist - 15 Years of Experience - Near 10583
Summary: Molecular Biologist with expertise in highly driven research environment experience ranging from writing grant proposal, MTAs with pharmaceutical companies, planning experiments, wet bench laboratory techniques, data collection, analysis, writing articles for publication in journals, preparation and presentation at National and International meetings to teaching and training students and fellows and supervising tec...
Tags for this Online Resume: Oncology, Research, Cancer, Pharmaceutical, Translation research, Medical writing, liaison, Management, Senior scientist, Clinical scientist, CRA, scientist, oncology, cancer research, medical liaison
Medical Scientist - 13 Years of Experience - Near 21136
HIGHLIGHTS OF QUALIFICATIONS: * 2+ years of clinical research monitoring experience and 25+ years pre-clinical experience * Knowledge of clinical trial procedures and approval processes. * In-depth knowledge of ICH GCP guidelines * Knowledge of FDA regulations * Knowledge of clinical trials for investigative biomedical and pharmaceutical studies. * Good working knowledge of Pharmacology, Epidemiology, Biology, Chemistry, Ph...
Tags for this Online Resume: Cancer, Leadership, Medical, Patient Care, Quality, Quality Assurance, Quality Control, Trauma, Troubleshooting, Phlebotomy
Medical & Clinical Laboratory Technician - 6 Years of Experience - Near 60706
SUMMARY OF QUALIFICATIONS * BA and Masters Degree in Bioengineering and Biotechnology from Poland * Motivated team player, detail oriented, result focused with excellent time management and people skills * Proficient in MS-Office (Word, Excel, ) and the internet * Strong knowledge of anatomy and physiology, medical terminology, ICH GCP guidelines * Proven ability to work efficiently and effectively under pressure * Versatil...
Tags for this Online Resume: Administrative Assistant, Documentation, Patient Care, Scheduling, Therapy, Management, Pathology, Protocol, Satellites, Polish/English
Clinical Regional Monitoring - 10 Years of Experience - Near 20912
20/20, Addis Ababa University (CRO), Addis Ababa, Ethiopia, March 2005 to July 2006 Senior Clinical Research Associate - Opthalmology Studies, National Blindness, Low-Vision & Trachoma * Oversaw $3.5M study across 14 regional states to explore blindness, low-vision, and trachoma demonstrated sharp organizational skills in managing team of clinical data managers verifying data, and performing systematic networking of databas...
Tags for this Online Resume: Clinical Research, Research, Protocol, Collection, Critical Care - Neurology, Management, Neurology, Oncology, Quality, Quality Assurance
Clinical Data Management - 1 Years of Experience - Near 07302
Tags for this Online Resume: Data Management, Clinical Trial, ICH-GCP, SOP, Clinical Data support, Clinical Trial associate, Entry level
Clinical Research - 12 Years of Experience - Near 78254
SUMMARY OF QUALIFICATIONS * Managed Phase I -IV and observational Clinical Research Trials for HIV/AIDS, HIV Vaccine trials, HIV and Hepatitis, Infectious Diseases, Hyperlipidemia, Diabetes, Renal CKD, Secondary Hyperparathyroidism, Vitamin D Deficiency, Diabetic Nephropathy, Allergies, Asthma, and Immunology, Hepatic therapeutical area, from HBV, HCV, Fatty Liver, Cirrhosis in the Liver, medical devices. * As an inhouse mo...
Tags for this Online Resume: PEDIATRIC, Pharmaceutical, Surgical, C Programming Language, Data Entry, Hepatitis, Hepatitis C, Research, Therapy, Cardiovascular
Clinical Research - 5 Years of Experience
Medical Doctor with Post Graduate training and Diploma in Clinical Research from AAPS Toronto * Over 14 years experience working in clinical environment. * Strong understanding of Clinical Research processes according to Study Protocols ICH/GCP
Tags for this Online Resume: Clinical Research, Management, Protocol, Research, Data Management, Good Clinical Practices, Medical, Clinical Trials, Informed Consent Forms, Study Reports, SOP, Regulatory approval
Project Manager
SUMMARY Experienced IT Software professional specialized in working with clients to understand and implement requirements and applications/systems to provide business analytics and strategic solutions in various roles as a Senior Business Analyst, Senior Project Manager, Senior SFDC Architect, Senior Program Manager/Product Manager and Senior Product Owner. Collaborate with product management, engineering and other cross-fu...
Ideal Companies: program mgnt
Tags for this Online Resume: Inventory, Support, Active Server Pages, Forecast, Forecasting, Oracle, Quality, Quality Assurance, Data Entry, Planning
Clinical Research - 3 Years of Experience - Near 02478
Summary: MS in Clinical Investigation with 3+ years of experience as Clinical research assistant cum coordinator seeking a preferably full time position in Clinical Research fields as Clinical Trial Associate / Project Management. Offering combination of strong background in biological sciences (specialization in Oncology, Molecular biology) as well as deep understanding and knowledge of ICH-GCP & FDA regulations. Demonstra...
Tags for this Online Resume: Clinical Research, Documentation, Research, Advertising, Audit, Budgetary, Data Entry, Data Management, Filing, Gastroenterology, Recruting, IRB admministration, regulatory, phase ii, clinical trials, ICH-E6 GCP and GLP, HIPAA compliance
Registered Nurse - 15 Years of Experience - Near 60030
SUMMARY OF EXPERIENCE * Monitored Phases I, II, III, clinical trials in many therapeutic areas, including, but not limited to, Oncology, Cardiology, Dermatology, Infectious Diseases, Immunology, Women's Health, Gastrointestinal, Genitourinary, Neuroscience, in Adult and Pediatric (Otitis Media and Influenza) populations. * Managed multiple studies in various stages of conduct at as many as 15 study centers at any given time...
Tags for this Online Resume: Cardiology, Clinical Research, Dermatology, Gastrointestinal, Good Clinical Practices, ICH, Immunology, Infectious Diseases, Monitoring, Oncology
Clinical Regional Monitoring - 17 Years of Experience - Near 46321
SUMMARY OF CLINICAL EXPERIENCE Eleven years' experience as a CRA which includes 2 years as a Lead CRA in clinical trial monitoring, including study start up, study initiation through closeout, as well experience in International, and Domestic studies. Provide on-site clinical trial monitoring and full site management at investigational sites in the conduct of Phase II-IV clinical trials. Recruited and trained CRA (s), inves...
Tags for this Online Resume: Data Management, Gastroenterology, Management, Patient Education, Pharmaceutical Industry, Start up, Clinical Research, Research
Clinical Regional Monitoring - 20 Years of Experience - Near 18929
Seeking an opportunity with a Pharmaceutical, Biotechnology company or CRO as a Senior Lead Clinical Research Associate, Lead CRA, CRA Manager/Trainer (Mentor) and/or CRO Oversight Monitor to employ my 27 years of clinical research monitoring, management skills and CRA mentoring as well as19 years of Respiratory/Pulmonary and Cardiopulmonary critical care clinical medicine. Clinical Research Experience: Projects/Therapeutic...
Tags for this Online Resume: Pharmaceutical, Clinical Research, Research, Rheumatology, Biomedical Industry, Pharmaceutical Industry, Cardiology, Critical Care - Neurology, Critical Care - Respiratory, Neurology, oncology, clinical, phase, gcp, protocol, trial, ich
