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Online Resumes with "Crf"
Clinical SAS Programming - 4+ Years of Experience - Near 43016
Experienced in SAS/BASE SAS/SQL, Assisted in CRF Annotation and edit check plans, experienced in offline listings, Good working knowledge on SDTM,CDISC Std. Good knowledge on Demography, concamitant medications, Medical History etc..
Tags for this Online Resume: Dublin,Ohio, SAS, BASE SAS, SDTM, CDISC, CLINICAL RESEARCH, ICH-GCP
Gis Engineer
GIS Executive Nokia L & C (Riding Engineers India Pvt. Ltd) Feb.2012 - at present Organization: NOKIA Location & Commerce (NOKIA L&C / NAVTEQ) as vendor. Designation: Geo Analyst(Geo-Coding) in GMP(Gurgaon Map Production) Team Company Profile: NAVTEQ / NOKIA L&C is the leading global provider of maps, traffic and location data (digital location content) e...
Tags for this Online Resume: Gis , Gis Engineer , Gis Executive
Clinical Research - 7 Years of Experience - Near 40009
Tags for this Online Resume: Source data verification, ICH GCP, Site monitoring, CRF review, Communication with site, Ethics committee and sponsor, compliance to protocol
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 - 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
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 In-house Monitoring - 4 Years of Experience
Seeking a position in a globally focused organization that will utilize my qualifications while offering several opportunities to integrate personal enrichment with professional goals.
Tags for this Online Resume: Clinical Research, ICH GCP Guidelines, Schedule Y, eCRF, EC Submission, Site coordination, Inspection, Project Coordination
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 - 2 Years of Experience - Near 77449
HIGHLIGHTS OF QUALIFICATIONS: * RN with close to 2-years experience in clinical trials monitoring * Knowledgeable of clinical trial procedures and approval processes. * In-depth knowledge of ICH GCP guidelines and FDA regulations * Conversant with Design and Review of case report forms (CRF) * Conversant with Site Monitoring visits (PSVs, SIVs, IMVs and COVs) to meet study expectations. * Clinical and post-marketing safety ...
Tags for this Online Resume: Direct Patient Care, DRESSING CHANGES, Medical, Patient Care, Suctioning, Surgical, Wound Care, Acquired Immune Deficiency Syndrome (AIDS), HIV, Monitoring
Clinical Research
Summary of Qualifications Clinical Research Manager, Associate, Monitor, Coordinator, with over 25 years experience in the medical field and 21 years experience in clinical trials with extensive experience in the fields of Cardiology, Electrophysiology, Neurology, Urology, Autoimmune, Respiratory, Gastroenterology, Weight Loss, Diabetes, Women's Studies, Arthritis, COPD, Gynecology, Endocrinology, Rheumatology and Stem Cell...
Tags for this Online Resume: Monitoring, Protocol, Cardiovascular, Clinical Research, Management, Pharmaceutical, Research, Therapy, Audit, Data Management, Medical Device, CRA, CTM, Clinical Trials
Team Leader - 9 Years of Experience - Near 08854
Experience Summary * A seasoned analytics and consulting professional with ~9 years of industry experience as a SAS Consultant and Business Data Analyst with a strong understanding of Data Handling and Management, SAS, Project management, and Business Analysis. Project Summary This program supports the in-out of the company's innovative value-based programs. This includes the analyses of business KPIs and financial metrics ...
Tags for this Online Resume: Programming, Support, ETL, QA, Management, Data Extraction, Project Management, Requirements Analysis, SAS, Data Analyst
