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Online Resumes with "clinical trial data"
Family or General Practitioner - Near 55124
PROFESSIONAL SUMMARY CLINICAL EXPERTISE: Demonstrate clinical expertise to serve as a resource for providers, clinical trial groups, and organizations in the scientific/medical arena Utilize medical knowledge to be a key presenter at various medical and scientific venues to provide national or international audiences with valuable clinical trial data Able to ensure/maintain comprehensive knowledge of current issues and new ...
Tags for this Online Resume: Marketing Management, Medical, Licensing, Management, Patient Care, Troubleshooting, Hardware Troubleshooting, Hardware/Systems, Health Care Industry, Leadership
Clinical Research - 1 Years of Experience - Near 27704
A goal-driven dependable and dedicated management professional with over 12 years' solid experience in Clinical Data Management operations at a non-profit organization. Has extensive knowledge of GCP ICH and FDA regulatory requirements regarding management of clinical trials data. Expertise in data management practices for paper studies as well as electronic data capture systems. Has a proven ability to effectively communic...
Tags for this Online Resume: Data Management, Email, Management, Query, Training, Documentation, Clinical Research, Compliance, Data Entry, Project Management
CRA - 20+ yrs. Healthe Care, 6+ yrs. Clinical Research
Tags for this Online Resume: Clinical Trial Associate, Clinical Research Associate, Document Specialist, Clinical Trial Data Management
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
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
Marketing - Near 94401
Summary of Qualifications Seeking a position in Medical Affairs/Medical Writing/Regulatory Affairs/Marketing/Publications: * Pharmaceutical, Medical Device, Biotech and High Tech industry management experience and training * Expertise in translating complex technical, scientific and medical information into internal and global customer communications strong client communication skills Experienced with literature reviews, se...
Tags for this Online Resume: Advertising, Management, Project Management, Statistical Analysis, Telemarketing, Billing, Budgeting, Certificate Authority, CMM (Capability Maturity Model), Coding
Analyst - 2 Years of Experience - Near 01880
& Provide SAS and other programming support with respect to design, conduct & Analysis of clinical trials. Create SAS analysis databases, summary tables and graphs for presentations, manuscripts and reports. Write and document SAS production macro code that can be used for a wide variety of applications. Develop SAS programs for statistical tables, data listings, and edit checks. Assist with Programming for editing and qual...
Tags for this Online Resume: SAP, Statistics, Protocol, Audit, Credit Card, Equities, IBM MVS Operating system, Job Control Language, Microsoft Windows NT, Public Health, clinical trials
Clinical SAS Programming - 20 Years of Experience - Near 98368
I am a SAS programmer looking for a remote, work from home position I recently moved to a remote area of the Olympic peninsula in the state of Washington, 2 hours west of Seattle. I am looking for a remote, work from home position as a clinical trials SAS programmer. I have experience in applying software engineering and risked-based quality assurance principles to develop a lean, efficient, modular, and well tested ...
Tags for this Online Resume: SAS, 21 CFR Part 11, software engineering, SAS Macros, Statistics, Oncology, manager, CDISC
Programmer Analyst - 8 Years of Experience - Near 22042
PROFESSIONAL SUMMARY * Over 8 years of experience in Information Technology field with strong emphasis in SAS Application Analyst/ Programmer with 3+ years of hands on experience and professional experience in Clinical Trial projects and also worked as Application Analyst in the CROs, Healthcare and Pharmaceutical industries. * Experience in analyzing and coordinating clinical data, generating detail summary reports and dat...
Tags for this Online Resume: Management, Oracle, Oracle 9i, Information Technology, Process Improvements, Coding, Health Care Industry, HyperText Markup Language, Manufacturing, sql, SAS analyst
Clinical Quality Assurance - 10 Years of Experience - Near 27571
Career Summary As a Senior Quality Control Analyst, I am responsible for planning, auditing, developing, documenting and implementing a quality framework for processes and associated training materials for Interactive Response Technology (IRT) and Electric Data Capture (EDC) systems. I also have experience as a Quality Control/Assurance Auditor. I have performed internal and external audits for validating clinical software,...
Tags for this Online Resume: Data Management, Management, Process Improvement, SAS, Documentation, Test, Test Cases, Data Entry, Database, Database Design
Statistical Programmer - 5 years Experience - US
Summary * Certified Base Programmer for SAS 9 with 5+ years of biostatistical programming experience in CRO, hospitals, pharmaceutical, and healthcare industries. * Involved in drug development process with experience in analyzing, reporting, and reviewing pre-clinical/clinical trial data. * Good understanding of FDA submission (IND, NDA) process, clinical protocols, CRFs, CDISC (SDTM, ADaM), 21 CFR Part 11, GCP, and IRB gu...
Tags for this Online Resume: SAS, Proc, Programming, Statistical Analysis, SAP, Research, Statistics, Structured Query Language, Management, Test
Clinical Data Management - 8 Years of Experience - Near 07083
SUMMARY * Senior Clinical Trial Data Manager with extensive experience in domestic and global trial data management * Deep expertise leading Phase I-IV trials, across various therapeutic areas, including Oncology, Cardiology, and Diabetes. * Adept at serving as the liaison between Sponsor and CRO/BPO. * Deep familiarity with ICH / GCP guidelines. Experienced with Medidata RAVE, and Oracle platforms, and likewise, skilled in...
Tags for this Online Resume: Clinical Research, Protocol, Research, Oncology, Audit, Management, Project Management, Data Manager, Rheumatology, Trend Analysis
