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Online Resumes with "Case Report Forms"
Clinical SAS Programming
SUMMARY OF QUALIFICATIONS * Certified SAS/Statistical programmer with over 7 years of experience in data analysis and statistical programming in phases I-IV of clinical trials working for Pharmaceutical companies and CROs in various therapeutic areas with high proficiency and within given timeline * Expertise in analyzing and coordinating clinical trial data, generating reports, tables, listings and graphs using SAS in acco...
Tags for this Online Resume: SAS, Proc, Programming, Data Management, Extensible Markup Language (XML), Generate Reports, HyperText Markup Language, Management, PDF, Pharmaceutical
Clinical Research
PROFESSIONAL SUMMARY: Experienced Clinical Research Professional seeking career advancement with a CRO where I can make a positive contribution by utilizing my clinical research expertise. In-depth knowledge of clinical trial policies and procedures, study protocols, GCP guidelines, ICH guidelines, regulatory clinical trial documentation requirements, IRB documents submittal, sponsor electronic data capture systems for data...
Tags for this Online Resume: Chemotherapy, Clinical Research, Collection, Gastrointestinal, Oncology, PEDIATRIC, Protocol, Support
Clinical SAS Programming
SUMMARY * A Certified SAS Programmer with over six years of working experience in SAS applications for Clinical Research and Analysis. * Experienced working with Pharmaceutical companies and CROs. * In depth experience and knowledge in various SAS products such as BASE /SAS, SAS /MACROS, SAS/STAT, SAS/ACCESS, SAS/SQL in Windows and UNIX environments. * Worked extensively by using base/SAS, SAS/macro, SAS procedures (proc so...
Ideal Companies: Mrs.
Tags for this Online Resume: Cancer, Protocol, SAP, SAS, Oncology, PDF, Proc, Programming, Statistical Analysis, Structured Query Language
Clinical Regional Monitoring - 15 Years of Experience - Near 75219
Professional Summary Accomplished and energetic Senior Clinical Research Associate with a solid history of achievement in monitoring clinical trials. Motivated leader with strong organizational and prioritization abilities. Performed lead study duties to include trip report review and expense reporting. Mentored junior level CRAs and provided feedback and constructive critiques. Interested in senior positions as a research ...
Ideal Companies: Allergan, Bayer, CMED, Novartis, Pfizer, Paidion Research,
Tags for this Online Resume: Clinical Research, Research, Medical, Medical Records, Monitoring, Documentation, Protocol, Complaints, Nursing, Ophthalmology
Clinical Research Project Manager Interested in Growing with a Patient Centered Organization
My career goal is to first obtain a clinical research project manager position with an innovative, patient-centered pharmaceutical company, medical device company, clinical research organization (CRO), or medical center. Eventually, I would like to prepare to segue into international development as a Senior Director and play an integral role in developing a research infrastructure for new companies and/or those interested ...
Ideal Companies: Pfizer, AstraZeneca, Becton Dickinson, etc.
Pharma/Drug Safety (Research, Development)
Highly experienced, trained research and drug safety professional with extensive knowledge of FDA, EU and ICH regulations necessary to develop, study, and market medical drugs and devices. Public health professional with over 15 years of proven experience as a general physician, direct outpatient care and emergency medicine provider. Passionate about global health and drug safety. Adept in research, grant writing, public he...
Ideal Companies: Abbott, Medix, PRA health sciences, Catawba Research, Medpace, Acelity, Bellicum Pharmaceuticals, Covance, US Prahs, Novartis, Bayer, Integrated Resources INC, The University of Texas Sothwestern, Baylor Scott & White Health, Abbvie
Tags for this Online Resume: Public Health, Clinical Research, Data Analysis, Pharmacovigilance, FDA regulations, drug/device research and development, clinical trials, risk management, regulatory compliance, French language, Spanish language
Not Listed - 0 Years of Experience
3-years' experience coordinating and assisting in clinical trials monitoring activities * Sound knowledge of Good Clinical Practices (ICH-GCP) and FDA regulations * Vast experience in billing and coding, data management, data entry, conducting billing practices, and other administrative tasks * Familiar with various computerized coding programs and electronic health records. * Advanced medical/scientific knowledge and medi...
Tags for this Online Resume: Insurance, Audit, Compliance, Clinical Research, Data Management, Documentation, Filing, Management, Monitoring, Research
