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Online Resumes with "cra"
Tags for this Online Resume: clinical operations, Quality Assurance, clinical research, clinical trials, vendor management, Study Start-Up / Activation, In-House CRA, regulatory, pharmaceutical, cro, phase iii, phase i, phase ii, Manager
I absolutely enjoy what I do and look forward to work every week. I know there will be challenges and problems that my team and I will have to solve. I enjoy this career because every day is different. Every study requires a different amount of care and expertise/experience. I love the organization that comes with this career. I love having my own studies and organize documents according to company SOP as well as my own way...
Tags for this Online Resume: Instant Messaging, Data Analysis, Document Management, Good Clinical Practices, Good Laboratory Practices, Management, Medical, Medical Terminology, Microsoft, Microsoft Excel, Data Entry, Site Feasibility, Trial Master File Audit, Trial Master File, Routine Monitoring Visits, Bilingual, IWRS Systems, DSMB, analysis of PK data from different generations of Japanese subjects, Receiving Plasma samples and storing them in freezers, Urine collection and UA testing, Phlobotemy, ECGs, Dosing, Writing Visit Reports, Query data sheets, Resolving Queries within the SOP allotted time frame, Pippetting Fluids and shipping off with appropriate courier., CRA visit matrixes, Reporting numbers and statistics to Project Manager and Operations Manager, Reviewing Source Documents and making original source documents according to procedures in the protocol, Protocol review sessions, QA sessions daily with a volunteer from each department to go over daily data and tasks to make sure none were missed, Call subjects and perform AE checks according to timelines on protocol, Send critical documents to sites directly or through CRAs as demanded., Make progress matrices of site visits and site reports, Send reminder emails for upcoming visits for CRAs and internal deliverables, Coder
Over 30 years' of international experience specialising in the oil gas and petrochemical industry. During the last 10 years I have held a senior HSSEQ management role with two major EPC contractors focussing on subsea activities project execution has covered FEED through to project realisation/commissioning. Throughout this period my responsibilities have been inclusive of the regional management of HSSEQ functions and ulti...
Professional Summary: * Certified clinical research professional with nearly 10 years of clinical research experience in the medical device industry. I have a wide range of knowledge with site and study management having worked as an In-house/Field CRA, Lead CRA and Clinical Trial Assistant. * Conducting: Qualification, Initiation and Close-Out monitoring visits for pre and post-market trials. * Start-up activities for both...
I am always in search of a management position with an exciting opportunity which will allow me to bring value to another company and assist in creating a successful business enterprise. Whereby I can actively utilize my entrepreneurial spirit and creative talents. I have 15 years of executive management experience adding value to start-ups and rapid growth companies. I possess excellent leadership, management, oral/writ...
SUMMARY: * A lifetime of working in the Healthcare Industry having served as a clinician, teacher, manager and researcher in acute and chronic care environments, transitioning into pharmaceutical, medical device industries and government agencies including National Institute of Health, National Institute of Child Health and the Department of Defense: Aviation-Space-US Air Force * Respiratory Therapy, across the human lifesp...
Manage day-to-day clinical operations of dermatology trials (Phases III - IV) * Coordinate and prioritize work load based on study timelines and protocol demands adam.m.haas@
I am looking for a permanent position as a Senior Clinical Research Associate/Lead CRA with an emphasis on Oncology studies.
Tags for this Online Resume: Clinical Research, Research, Cancer, Clinical Operations, Oncology, clinical research, monitor, senior clinical research associate, clinical, phase iii, phase iv, phase ii, phase i, clinical trials, pharmaceutical, cro, regulatory
PROFESSIONAL SUMMARY: Experienced Clinical Research Professional seeking career advancement with a CRO where I can make a positive contribution by utilizing my clinical research expertise. In-depth knowledge of clinical trial policies and procedures, study protocols, GCP guidelines, ICH guidelines, regulatory clinical trial documentation requirements, IRB documents submittal, sponsor electronic data capture systems for data...
SUMMARY * 23 years as a Clinical Data Management working for the following companies: Novartis, PRA International, Abbott, Covidien, Ingenix (i3), Ortho Clinical Diagnostics, Octagon Research Solutions and Pharmanet i-3. * 20+ years' experience of team leadership working with: Data Manager, Clinical Data Coordinator (CDC), Data Entry Personnel, Biostatisticians, Programmers, Investigators and Clinical Research Associates (C...
Summary of Qualifications: Over nine years as CRA and ten years as CCRC performing site management of phases I-IV clinical trials with large and mid-sized pharmaceutical sponsors and international CROs: INC Research/inVentiv Health Clinical, Pfizer, United Therapeutics Inc., Clinipace Worldwide (Formerly Paragon Biomedical), GeNO LLC, PAREXEL, Merck, Astra Zeneca/MedImmune, GlaxoSmithKline Actelion, Gilead Sciences, INO The...
My objective is to expand my career, with my long clinical experience and extended academic knowledge I am sure that I can be of great benifit and growth for the company that I will work for.I am looking for CRA position or drug safety position.