CV, Curriculum Vitae and Online Resumes Search
Recruiters - Try Postings!
Postings.com™ is a must-have for recruiters who want to:
- Find Qualified Candidates
- Find Job orders and Post Splits
- Be Found in Search Engines
- Implement a Social Sourcing Strategy
Job Seekers - Look Here!
Hitting a wall with your job search? Try Climber Premium.
- Top the Search Engines
- Unsurpassed Candidate Marketing
- Power Career Networking
- Fresh Jobs from the Net
Were you looking for Phase-I- job results?
Click Here to search for Phase-I- in our 2.4M jobs.
Online Resumes with "Phase I "
Clinical Research - 20 Years of Experience - Near 07081
Vaud. L'Hôpital Cantonal de Fribourg Performed and led all start-up aspects for a Phase II multi-center study for Crohn's disease. Monitored 120 patients using a PAF antagonist for asthma, including pre-study visits, site initiations, monitoring, and close down. Wrote protocol and designed CRF for a methacholine challenge study. Monitored pharmacokinetic Phase I studies co-wrote final study report.
Tags for this Online Resume: Clinical Research, Research, C Programming Language, Consulting, Hepatitis, Hepatitis C, Pharmaceutical, Protocol, Filing, Health Insurance Portability And Accountability Act
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
Biostatatician - 6 Years of Experience - Near 46802
Professional Summary: * SAS Certified Programmer with around 6 years of experience in clinical trials data analysis and reporting in Health care and Pharmaceutical fields. * Well-versed with clinical data analysis: analyzing clinical data, creating tables, listing and generating reports and graphs as per requirements, specifications and Statistical Analysis Plan (SAP). Experienced with SAS procedures such as Proc Format, Pr...
Tags for this Online Resume: Protocol, SAP, Clarify, Data Analysis, Documentation, ETL, Extensible Markup Language (XML), Extract Transform Load Tools
Clinical Research
SUMMARY: * POST-MARKETING REPORTING: Vast clinical experience in reporting post-marketing events in the pharmaceutical industry. * CDM: Acquaintance on clinical data management, pre-clinical and clinical trials (Phase I, II, III and IV) * CLINICAL WRITING & DOCUMENTATION: Create clinical project documents according to the protocol, including, but not limited to, source documentation forms and guidelines, monitoring Standard...
Tags for this Online Resume: Ipc, Planning, Protocol, Research, Reuters, Business Planning, Coding, Documentation, Immunology, Information Technology
Clinical Project Manager
Accomplished, dynamic professional experienced in synergizing communications between clinical research centers, contract research organizations (CROs), and major pharmaceutical corporations to amass clinical investigation objectives. Adept at executing, managing and monitoring IRB-approved, Phase I-III clinical studies and data management. Proven success in identifying opportunities to improve timely event reporting, increa...
Tags for this Online Resume: Clinical Project Manager, Clinical Team Lead, Clinical Research Manager, Clinical Research Associate
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
Hazardous Materials Removal Worker
PROFESSIONAL SUMMARY Mr. Malakieh has more than 14 years of experience in the environmental, industrial hygiene, and asbestos management field. Mr. Malakieh is experienced in indoor air quality assessments, asbestos surveys, asbestos abatement project design and management, and Phase I environmental site assessments. Mr. Malakieh has extensive experience in the area of industrial hygiene air monitoring, and air environment ...
Tags for this Online Resume: Project Management, Project Manager, Monitoring, Consulting, Management, Surveys, Services, Engineering, PCM, Pulse Code Modulation (PCM)
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
Instructional Coordinator
Tags for this Online Resume: Instructional Design, Business Analyst, Technical Writer, Leadership, Performance Consultant, Consultant, System Design, ISD, Program Manager, Health, Safety, Environment, HSE, Instructional Systems Design, Manager, Project Manager, Team Lead, Documentation Coordinating, Curriculum Development, Editing, Adobe Captivate 9, Articulate, Storyline, MicroSoft Office Suite, Visio, LMS, LCMS, Houston, TX, 77035, remote, Instructional Systems Design Manager, eLearning, Mentoring, Budgeting, Adult Learning, Innovative Learning Strategies, Consulting, Strategic Planning, Training, Development, Team Leadership, Team Development, Design Consistent Training Experiences, Process Improvement, ADDIE, Hands-On Application Based Training, Curriculum Design, Learning Management Systems, Visual Oral / Design Courses, Virtual In-Personal Training, Instructional Design Projects, Performance Management, Client Relations, Needs Assessment, Blended Learning Experiences, Customer Service, Training Industry Trends, Metrics Design, Documentation, Target Audience Learning, Web-Based Applications, Team Oriented Environment
Developer - 7 Years of Experience
PROFESSIONAL SUMMARY * Over 9 years of Clinical SAS programming experience in a Pharmaceutical industry involving different Phases (I, II & III) of clinical trials. * Experienced in working closely with statisticians to provide SAS programming in analyzing clinical trials data and generating Statistical Analysis Files, Tables, Listings, Summaries and Graphs/Figures (TLFs) for the Integrated Summary of Safety (ISS) and Integ...
Tags for this Online Resume: Microsoft Windows, SAS, Structured Query Language, Unix, Microsoft Windows 7, Windows 7, PDF, Proc, Extensible Markup Language (XML), Microsoft Excel
