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Online Resumes with "Clinical trials"
Clinical Research - 20 Years of Experience - Near 91354
QUALIFICATION SUMMARY Multi-center clinical trial Staff management and Budget development and fiscal research contracts development management Nationally recognized in Proposal & grant writing Revenue generation contraceptive development Contract negotiation International partnerships Federal regulatory compliance Fiscal oversight including Board of Directors relations, Multimedia recruitment company 401K and space committe...
Tags for this Online Resume: Evaluate, Gynecology, Obstetrics, Publications, Clinical Research, Research, clinical, phase iii, phase iv, phase i, clinical trials, research, cro, regulatory, phase ii, pharmaceutical
Clinical Research - 11 Years of Experience - Near 20774
My goal is to successfully coordinate both the technical and administrative details of any research assignment collaborating with the Principal Investigator to achieve study integrity and objectivity through the successful implementation and completion of protocols and procedures. Self-motivated achiever with over eight years' experience in different areas of research work including Human Participants in Research both for C...
Tags for this Online Resume: Clinical Research, Compliance, Good Clinical Practices, Health Care Industry, Health Insurance Portability And Accountability Act, HIPAA compliance, Pharmaceutical, Research, Training
Quality Assurance Specialist - 13 Years of Experience - Near 08540
Professional Summary More than 14 years of experience in Pharmaceutical and Life Sciences Industry with key focus in Business Requirements Analysis Data Analysis and Management Software Application Testing Document Management Change Control and Release Management FDA Compliance Verification and Validation Quality Assurance Processes and Methodologies Developing Testing Strategies and Test Plans Test Scenarios and executing ...
Tags for this Online Resume: Test Scripts, Test, Management, Test Cases, Structured Query Language, Audit, CFR Part 11, Test Plan, Application Server, Documentation, validation of protocols
Project Manager - 20 Years of Experience - Near 18020
Summary Over 20 years of business relationship management with a focus on IT project management & operations management. Currently responsible for major pharmaceutical global accounts. Implementing and supporting Medidata full suite of applications. Pragmatic, hands-on global information technology leader with proven experience in the design, deployment and support of strategic enterprise-scale business technology solutions...
Tags for this Online Resume: Planning, Application Server, Budgeting, Citrix, Desk Top Support, Enterprise Requirements Planning, ERP Systems, Gateway, Infrastructure, Infrastructure Project Management, Associate Director project management, Associate Directory Clinicals, Clinical Trials, Medidata
Scientific writer - 8 Years of Experience - Anywhere in the US
I am a highly motivated professional seeking to utilize my technical, educational, creative and interpersonal skills to advance organizational goals and contribute to making real-world impacts in the scientific, pharmaceutical and research industry.
Tags for this Online Resume: Health Care Industry, Research, Pathology, Pharmaceutical, Public Health, Training, clinical, research, pharmaceutical, phase i, regulatory, clinical trials
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 Research - 15 Years of Experience - Near 77345
Professional Summary: A highly skilled professional having experience in managing projects delivering Health Economics and Outcomes Research (HEOR) modeling and analytic solutions. Worked as a Director of Project Management responsible for conducting epidemiological studies and clinical trials on cancer outcomes for pharmaceutical customers. Conducted research and analyzed scientific literature related to pharmaceutical iss...
Tags for this Online Resume: Statistical Analysis, Research, Management, Programming, Risk Assessment, Support, Technical Requirements, Account Management, Immunology, Pharmaceutical
Clinical Quality Assurance
SUMMARY * 20+ years of experience in Quality Management and continuous improvement of quality, within Drug Safety, Clinical, Manufacturing, Regulatory Compliance and R &D domains of Bio-Pharmaceuticals * Conducted risk based Investigator site global audits including contract global central clinical labs * Conducted and Managed CRO's, 3rd party vendors / service providers for GCP and GvP compliance * Supported Internal and e...
Tags for this Online Resume: Services, Compliance, Infrastructure, Link Access Procedure (LAP), Research and Development, SDLC, Test, Packaging, Product Development, Quality
Dental Assistant - 5 Years of Experience - Near 08820
Summary Highly skilled medical doctor with more than 15 years medical knowledge in various therapeutic area. 5 years' experience as Clinical Data Manager ensuring that data for clinical trials is properly collected, validated and clean. Diligently evaluate data, verify results and present conclusions. Excellent track record when it comes to consistent quality and reliability in carrying out research duties according to regu...
Tags for this Online Resume: Coding, Data Management, Data Quality, Database, Management, Quality, Quality Assurance, Data Analysis, Data Entry, Oracle
Clinical Regulatory Affairs - 1 Years of Experience
Tags for this Online Resume: Adobe Acrobat, Documentation, Good Clinical Practices, Regualtory Affairs, Clinical Trials, Clinical Research Coordinator, Regulatory Affairs Associate
Clinical Research Coordinator/ Associate
Applying to provide my services in Clinical Trials as a Clinical Research Coordinator/Associate
Clinical Research - 8 Years of Experience - Near 84105
Tags for this Online Resume: Accounting, Management, Payroll, Security, Licensing, Medical, Medical Records, Gastrointestinal, Cancer, Database, clinical, phase i, phase ii, clinical trials, research, cro, regulatory, pharmaceutical, phase iii, manage
