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Were you looking for Phase-I-IV job results?
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Online Resumes with "Phase I IV"
Clinical Research - 2 Years of Experience - Near 30344
Serve as a Clinical Research coordinator managing Phase I-IV clinical trials in any therapeutic area
Tags for this Online Resume: Consent, Recruit, OnCore, CRF, North Carolina, phlebotomy, monitor
Clinical Research - 2 Years of Experience
SUMMARY OF EXPERIENCE Over 3 years of experience of clinical research experience with a clinical research organization. Established a reliable consultants building relationships with a strong commitment to quality. Team oriented, strong organizational skills with attention to detail Phase I-IV Experience. Ability to perform SWAT, PSSVs, SIVs, IMVs, and COVs according to company timeline and deadline. THERAPEAUTIC AREA OF EX...
Tags for this Online Resume: Management, Protocol, Clinical Research, Documentation, Research, Cardiology, Corrective Actions, Data Analysis
Clinical Regulatory Affairs
Experienced and highly qualified Clinical Research Associate with over 10 years of experience in researching and knowledge of study startup, monitoring, and regulatory processes in the Pharmaceutical Industry. Highly proficient in performing quality assurance control on laboratory best practices while leveraging R&D experience to consistently achieve goals. Extremely focused and results-oriented in supporting complex, deadl...
Tags for this Online Resume: Data Management, Documentation, Management, Systems Administrator, Clinical Research, Health Insurance Portability And Accountability Act, Research, Project Management, Project Manager, Protocol
Clinical Data Analyst/Coordinator
Clinical Data Management Services, with extensive phase I-IV pharmaceutical experience in the following therapeutic areas: Dermatologic, Pathologic, Oncology, Ophthalmic, Infectious Diseases. Excellent analytical skills in data review and experience validation of data base design and study start up. Hands on knowledge of medical clinical research terminology and transcription, (EDC) Electronic Data Capture Experience.
Tags for this Online Resume: Clinical Data Coordinator, Clinical Data Analyst, Clinical Associate, Data Entry Operator, QA , Data Validation, Data Entry, Data Processor
Clinical Data Management - 9 Years of Experience - Near 01821
SUMMARY * I am certified-RAVE Study Builder- Certification Sponsored by Cognizant & Medidata USA. I have 12 years of experience in Project Management, Clinical Data Management, Technical Support and Team Management,Overall 10 years of progressive experience in Clinical Data Management domain from study start up till DBL activities. I am experienced with all aspects of data management including project management, edit check...
Tags for this Online Resume: Management, Data Management, Pharmaceutical Industry, Quality, Quality Control, Team Lead, Document Management, Audit, Training, Quality Assurance
Clinical Research - 10 Years of Experience - Near M1T3N
SUMMARY: * NIH trained Study/Site Coordinator with 10 years of experience in clinical research coordination and administration. * Demonstrated ability in coordinating & implementing Network / Pharmaceutical / Investigator-driven multisite Phase I - IV clinical studies. * Adept in liaising with internal and external stakeholders.
Tags for this Online Resume: Protocol, Clinical Research Associate, Infectious Diseases, ICHGCP, Logistics of study material, Monitoring, Data Entry, Team Lead, Essential Documentation, Informed Consent, SOPs, Coordinator, Regulatory, QA/QC, Source Docmentation, CRF's, TMF, EDC, Toronto, Contracts, SAE
Clinical Research - 20 Years of Experience - Near 34491
Coordinator on 100+ Phase I-IV Clinical Trials Indications pain general medicine gastrointestinal immunological rheumatology neurological orthopedic cardiovascular pulmonary contraceptive infectious diseases urology oncology
Tags for this Online Resume: Immunology, Cardiopulmonary resuscitation (CPR), Data Entry, REGULATORY SPECIALIST, CLINICAL RESEARCH COORDINATOR, UROLOGY/ONCOLOGY, NEUROLOGY
Clinical Research - 16 Years of Experience - Near 27616
PROFILE Senior Pharmacovigilance Officer with 10 years of experience in the Pharmacovigilance industry. Over the course of my career, I have been involved in Global/UK/European/US Phase I-IV studies covering a wide range of therapeutic areas to include infectious disease, oncology, neurology and cardiology. Specific areas of oncology include Non-Hodgkin's Lymphoma, cervical cancer, breast cancer, prostate cancer, hepatocell...
Tags for this Online Resume: Coding, Troubleshooting, Documentation, Oncology, Cancer, Cardiology, Critical Care - Neurology, Diagnostics, Hepatitis, Hepatitis B
Clinical Pharmacovigilance/Drug Safety
HIGHLIGHTS OF QUALIFICATIONS * A physician with more than 10 years medical training and clinical practice in Internal Medicine with a subspecialization in Cardiology in China. * Broad understanding of and experience in clinical medicine with strong medical judgment. 10 years medical training and clinical practice in internal medicine with a subspecialty in cardiology in China. * As an internal medicine resident completed tr...
Tags for this Online Resume: Safety Physician, Individual Case Safety Report (ICSR), Medical Review, Signal Detection, Data Mining, New Jersey, East PA
Vendor
PROFILE A seasoned executive with a wide breadth of experience in corporate and business development, finance and management planning, the development and implementation of corporate structure and strategy formulation. * Intimate knowledge of biotechnology-pharmaceutical industry with 15 year's experience in Life Science Companies and Contract Research Organizations (CROs). * Expertise in Phase I-IV clinical trials and tech...
Tags for this Online Resume: Clinical Research, Communications, Equity, Consultant, Financial Services, Business Development, Biotechnology, Pharmaceutical, FACETS, Management
Clinical Research - 8 Years of Experience - Near 60169
Professional Summary A certified professional Clinical Research with 4 years of experience in Clinical Research coordination and a year experience as Clinical Study Associate. Expertise in QC of documents, remote Monitoring and supporting the management by handling the tasks of multiple clinical research studies managing eTMF's & designing Clinical Portfolio's from Sponsor end. Expert in liaising between different departmen...
Tags for this Online Resume: Document Management, Monitoring - Remote and onsite, Clinical Research coordinator, Device trials, clinical Research, Project Management, QC and QA, Pharmacovigilance, Ethics and compliance, regulatory, Clinical study Associate, Multiple therapeutic areas experience, Phase 1-4 trials, Audits and Inspection readiness, Multiple software and application experience - Veeva VAULT , Impact , Quest , Sentinel,Tesla, EDC experience- RAVE Medidata, IRT system experience Clinpace , Endpoint
Clinical Research - 20 Years of Experience - Near 20882
Summary: Over 16 years managing clinical trials and data collection activities. Manage as Point of contact for sponsors, project teams, and investigational sites to facilitate clinical studies Phase I-IV. Responsible for the review and approval of case report forms, electronic data capture systems, review of protocols, implementing study procedure manuals, and monitoring plans. Additionally manage site selection, study exec...
Tags for this Online Resume: Collection, Quality Assurance, Test, Process Improvement, Project Management, Project Manager, Business Requirements, Clinical Research, Data Entry, Filing
