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Online Resumes with "Phase I IV"
Clinical Research - 1 Years of Experience - Near M1W 2T1
Foreign-trained medical doctor and clinical research professional with CRA Professional Development Clinical Site Monitoring & ICH GCP Training. Experienced in clinical study files review to ensure accuracy of all the documented data including ME & AEs. Comprehensive knowledge of clinical research methodology and proficient in Phase I-IV clinical studies and ICF processing and study protocols. Excellent time management and ...
Tags for this Online Resume: Toronto, Canada, Strong Clinical Trials & Medical Management background, Detail Oriented, Data Review, Clinical Trials Supervision, Team player, Quick Learner, Certified CR Professional with Medical Background, Compliance, Documentation, clinical, research, phase i, phase ii, clinical trials, phase iv, pharmaceutical, cro
Dental Assistant - 5 Years of Experience - Near 08820
Summary Highly skilled medical doctor with more than 15 years medical knowledge in various therapeutic area. 5 years' experience as Clinical Data Manager ensuring that data for clinical trials is properly collected, validated and clean. Diligently evaluate data, verify results and present conclusions. Excellent track record when it comes to consistent quality and reliability in carrying out research duties according to regu...
Tags for this Online Resume: Coding, Data Management, Data Quality, Database, Management, Quality, Quality Assurance, Data Analysis, Data Entry, Oracle
Clinical Research - 7 Years of Experience - Near 29483
PROFESSIONAL SUMMARY: Skilled Junior Clinical Trial Manager (Project Manager) and Clinical Research Associate with an excellent track record of success in Phase I-IV, Hematology, Oncology, Urology, Compassionate usage, Observational, Retrospective, and Device clinical trials. Post graduate degree in Clini- cal Research Administration with additional certification from Project Management (PMP), SoCRA (CCRP), and IAOCR. Solid...
Tags for this Online Resume: Protocol, Monitoring, Management, Oncology, Audit, Clinical Research, Data Management, Distribution, Documentation, ICH, project management
Clinical Research - 9 Years of Experience - Near 1
Liliana Andrea Sánchez Valencia is a Clinical Research Associate Sr. CRA at Inventiv Health Clinical Colombia S.A.S, based in Bogotá Colombia, where she completes project activities associated with monitoring functions of Phase I-IV clinical research studies while continuing to develop knowledge of the drug development process, Good Clinical Practices, and relevant regulations. Ms. Sánchez has therapeutic experience in the ...
Tags for this Online Resume: Clinical Research, Management, Research, Protocol, Query, Project Management, Project Manager, Documentation
Clinical Research - 12 Years of Experience - Near 32837
Profile: Clinical Research Professional with vast experience in Phases I- IV study trials in Oncology,
Tags for this Online Resume: Protocol, Good Clinical Practices, Quality Assurance, Test, Oncology, Management, Research, Clinical Research, Data Management, Phlebotomy, clinical, phase, trial, pharmaceutical, gcp, protocol, ich
Clinical Research - 10 Years of Experience - Near 08002
PROFESSIONAL SUMMARY * Research Nurse with over 10 years' experience * Therapeutic areas of experience include Cardiovascular, Oncology, Medical Device, Immunology, Pediatrics, Neurology, Rheumatology, Phases I-IV. * Skilled with sponsor and Investigator-initiated research projects * Multiple site management dealing with Europe, Asia, South America * Team Lead responsible for oversight of clinical research staff, time manag...
Tags for this Online Resume: Protocol, Research, Management, Documentation, Cardiology, Audit, Budgeting, Clinical Research, Critical Care - Neurology, Data Entry
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
Registered Nurse - 20 Years of Experience - Near 19111
Areas of Expertise * Bilingual- Spanish * School nursing * JCAHO/HIPAA Compliance * Phase I-IV Research Coordinator * DOT & IATA/IACO compliance * Basic & Advanced Life Support * Outpatient Ambulatory Care * Taking & Recording Vitals * Electronic Medical Record * HIV Rapid Test Certified * Patient/Student Education & Support * Medication Administration * Blood Draws
Tags for this Online Resume: rn, registered nurse, healthcare, nurse, Nursing, Assessments, DRESSING CHANGES, Medication Administration, Radiology, Surgical, nursing
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 SAS Programming
SUMMARY: Over Nine years of experience in SAS programming with good knowledge of advanced statistical methodologies applied in Pharmaceutical and Biotech industries. Expertise in analyzing and reporting various phases (Phase I-IV) Of Clinical Trials using tools like Base SAS, SAS/STAT, SAS/GRAPH, SAS/SQL, SAS/MACRO, SAS/ACCESS and SAS/ODSin UNIX and Windows environment. Developing Debugging and validating the project-specif...
Tags for this Online Resume: Programming, Support, Microsoft Windows, SAS, SAS/STAT, Data Management, Management, HyperText Markup Language, Oncology, Macro (Predefined Code)
Clinical Regional Monitoring
Summary of Qualifications: Over nine years as CRA and ten years as CCRC performing site management of phases I-IV clinical trials with large and mid-sized pharmaceutical sponsors and international CROs: INC Research/inVentiv Health Clinical, Pfizer, United Therapeutics Inc., Clinipace Worldwide (Formerly Paragon Biomedical), GeNO LLC, PAREXEL, Merck, Astra Zeneca/MedImmune, GlaxoSmithKline Actelion, Gilead Sciences, INO The...
Tags for this Online Resume: Management, Pulmonary, Clinical Research, Documentation, Research, Protocol, Allergy, Applications, Assessments, Biomedical Industry
Clinical Research - 15 Years of Experience - Near 54901
Summary Seasoned director of clinical operation and project management with over 18 years' experience in local and global CRO and pharmaceutical industry, specializing in phase I, BA/BE start-up operations. Complete and solid understanding of business priorities, genuine team player committed to managing operations and projects efficiently and without flaws, while contributing to revenue producing activities. Serve as a key...
Tags for this Online Resume: Clinical Research, Research, Dermatology, Support, Clinical Management, Documentation, Management, Ophthalmology, Outsourcing, Cardiology
