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Online Resumes with "Study Start up"
Clinical Research - 3 Years of Experience
Summary * Highly qualified clinical research professional with over 17 years' experience, including Phase I-IV domestic and international studies (including EU, Eastern EU, South America, Asia, and Canada) in a wide range of therapeutic areas. * Experienced in all stages of study development from start up to close out with ability to view study progress by each data point or from a more global prospective. * Skilled at effe...
Tags for this Online Resume: Clinical Research, Oncology, PEDIATRIC
Clinical Research - 16 Years of Experience - Near 94547
SUMMARY of QUALIFICATIONS 16 years of experience as a Clinical Research professional in Biotech and Pharmaceutical industries. Well-rounded skill, as a CRA in Clinical Operations processes, Clinical Development, Regulatory, TMF and Data Management. Skilled in data audit/review Study start up, Study conduct, Vendor management, and Site monitoring activities extensive knowledge of GCP-ICH, GLP, GMP guidelines familiar with Ex...
Tags for this Online Resume: Protocol, Assessments, Audit, Clinical Research, Documentation, Pediatrics, Research, Clinical Management, Distribution, oncology, phase, trial, clinical, protocol, pharmaceutical, gcp, ich
Clinical Research - 20 Years of Experience - Near 27517
SUMMARY Clinical Research Professional with more than 20 years experience in Phase II-IV clinical site management, regulatory compliance and monitor training for major pharmaceutical companies. Demonstrated expertise in electronic systems including CTMS, EDC, IVRS, CRF design, query management and corporate communications. Proven success in all aspects of clinical trials from study start up through close out in phase IIb-IV...
Tags for this Online Resume: Protocol, Clinical Research, Research, Audit, Training, Clinical Research Associate
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
Psychology - 17 Years of Experience - Near 92057
Clinical Assisted Director of Operations in the daily operation of all trials at the Site. Responsible for staffing and training study personnel and planning study start-up activities. Responsible for team performance and annual goal reviews. Responsible for client relationships through obtaining feedback from trial monitors and sponsors. Trials was an outpatient Phase 2-4 clinical research facility with a 4-bed sleep labor...
Tags for this Online Resume: Management, Process Improvements, Risk Management, Clinical Operations, Clinical Research, Research, Pharmaceutical, clinical, phase iv, phase iii, pharmaceutical, quality, clinical QA, GCP, document control, clinical trials, IRB, consent document, essential documents, nonessential documents, SOPs, Work Instructions
Clinical Operations Manager - 6 years experience - North Carolina
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
Clinical Trial Associate
To obtain a position in the clinical research field. An area which I am passionate about. Which will allow me to utilize my administrative skill as it pertains to study start-up.
Tags for this Online Resume: Management, Filing, Documentation, Budgetary, CVS, Document Management, Medical, Medical License, Clinical Research, clinical, trial, protocol, pharmaceutical, oncology, customer service, call center, customer service representative
Quality Coordinator
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...
Tags for this Online Resume: Documentation, Management, Data Management, Budgeting, Clinical Operations, Clinical Research, Collection, Compliance, Contract Negotiations, Distribution
Clinical Research
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...
Tags for this Online Resume: Chemotherapy, Clinical Research, Collection, Gastrointestinal, Oncology, PEDIATRIC, Protocol, Support
Clinical Research - 20 Years of Experience - Near 30016
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...
Tags for this Online Resume: clinical , Data, Manage , Reasar, Data Manager, Query, Coding, Quality Assurance, Test, Medical, Audit, Clinical Research
Clinical Research
SUMMARY: * rn, bsn, cpm, * Over 28 years of Clinical Research experience * Respiratory, Ophthalmology, Oncology, Infectious Disease, Cardiovascular, CNS and Gastrointestinal * Phase I, II and III experiences * 14 years of Clinical Trial/Project Management experience * 4 years of field monitoring experience * 14 years of experience providing oversight to CTAs and CRAs PurDue PharmA July 2017 - present Sr Clinical Project Man...
Tags for this Online Resume: Clinical Research, Research, Distribution, Project Management, Project Manager, Integrated Development Environments, Protocol, sheets, Management, Biomedical Industry
Clinical Research
Tags for this Online Resume: Database, Construct (App Dev Tool), Data Analysis, Oncology, Data Entry, Support, Cancer, Cardiovascular, Data Queries, Start up
