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Online Resumes with "eCRF"
Clinical Trial Leader - 9 years in industry - edc, ecrf, ivrs, sop, gcp, ccra, data quality, SAE
I have strong clinical research industry qualifications. I am seeking a position that is either in Richmond VA or can be done from my home office. I have been part of many successful projects and look forward to future successes!
Senior Clinical Data Manager
Over 15 years of broad knowledge and experience in clinical database and project management activities in Roche pharmaceutical company. A result-oriented professional who effectively meet project commitment with strong interpersonal communications and ability to interface well with all level of organization. Mentors and support members of study management group. Highly skilled in EDC (Rave) and Oracle clinical data manageme...
Tags for this Online Resume: Medidata Rave, Oracle Clinical, Hyperion, Spotfire, Excel, Word
Experienced Research Professional seeks CRA position!
Passionate, hard-working, intelligent, leader, compassionate, organized
Ideal Companies: I would enjoy working with any CRO or Sponsor who values and rewards excellence and a strong work ethic from their employees.
Tags for this Online Resume: Clinical Research Associate, CRA, Regulatory, Monitor, Auditor, GCPs
Clinical Data Manager - India - 7 Years Exp. - Very Very Quick Learner
Overall 6.9 years of experience in Clinical Data Management. Broad experience in Data Management which includes Data Validation, Query Initiation, Client Interaction (Face-To-Face or WebEX), Reviewing of important Documents (Protocol, eCRF, Electronic Specifications, Data Entry Guidelines etc). Highly efficient and skilled at providing coaching and guidance to Internal and External Clients.Very Fluent in English.Excellent i...
Clinical Research Associate
John is detail oriented, highly dependable previous site monitor and study coordinator with 4 years and 6 months experience, including assistant project management in the pharmaceutical development industry He has attained knowledge and experience in 4 years of hands on provision of care for elderly and disabled persons assisting them with activities of independent daily living as well as dealing with transitional aspec...
Ideal Companies: Alcon, Merck, Wythe, Pfizer, Bristol-Meyers Squibb, Covance
Tags for this Online Resume: in-house monitor, Clinical Research Associate
Scientific Programmer - 6 years Pharma/CRO Experience - Philadelphia
Tags for this Online Resume: CDISC SDTM, SAS Certified, Analyst, Clinical Data Management, Inform eCRF, CDR Metadata
Clinical Research - 7 Years of Experience - Near m9w4v
COVER LETTER: Dear Sir/madam, It's my greatest pleasure to apply for the position of Research Assisatnt. I believe that my experience and skills will prove useful to your organization. I hope that you carefully review my qualifications and skills displayed in this letter and the resume attached to it. The amalgamation of my appropriate education and related experience has provided me with all the unique skills and qualifica...
Tags for this Online Resume: Transcription, Clinical Research, Documentation, Immunization, Management, Medical, Protocol, Quality Assurance
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
General - 1 Years of Experience - Near 18944
Summary of qualifications Highly effective in promoting a positive, productive environment. Developed innovative programs for major eClinical firms, incorporating trends on the leading edge of data management and eCRF design in the clinical research industry. Well organized and focused in coordinating projects for self and others. Skilled and thorough in analyzing problem situations and finding creative solutions. Advocate ...
Tags for this Online Resume: Standards, Process Improvement, Competitive Analysis, Product Management, Data Management, Management, Program Management, Project Management, Thought Leader, Requirements Definition
Biochemist - 1 Years of Experience
Summary of Qualifications * Master degree in Science with more than 15 years' experience in educational and research setting. * Good knowledge of Ontario health care system and OHIP rules. * Very good knowledge of GCP, TCPS and procedures required for REB documentation. * Good computer skills on Microsoft Office programs and e-CRFs * Very good knowledge of research procedures as obtaining informed consent, drug accountabili...
Tags for this Online Resume: Coding, Research, Training, Accounting, Administrative Assistant, Communication Skills, Documentation, Good Clinical Practices, Data Entry, Data Management
Quality Coordinator - 6 Years of Experience - Near 60504
PROFESSIONAL SUMMARY: * Total of 9.5 years of experience in Health Care industry. 6 years' experience in Clinical Data Management. * Worked as a Clinical Data Coordinator in Quintiles Technologies from Feb 2011 to Aug 2014. * Worked as a Clinical Data analyst in PAREXEL International from Aug 2008 to Feb 2011. * Also, I have 3.5 years of experiences in Medical Microbiology field in health care sector I started my career as ...
Tags for this Online Resume: Data Management, Health Care Industry, Management, Microbiology, physical therapist
Postsecondary Teacher - 11 Years of Experience - Near 29376
CURRICULUM VITAE: Sharon Woodruff Team excellence instructor, facilitator, and trainer. Proven managerial, interpersonal, and training skills. Work History Title: Senior Clinical Research Associate Company/Location United BioSource Corporation Kansas City, MO/Regional United States Dates July 2014 - January 2015 Accountabilities Implement and monitor clinical trials for medications and devices to ensure sponsor and invest...
Tags for this Online Resume: South Carolina, Training, New Hire , Business, Education, Postsecondary, Excellence
