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Online Resumes with "Clinical Trial"
Senior Identity Access Management - 2 years experience - New Jersey
ITIL and Six Sigma certified; accomplished Senior IAM Technical Analyst with over a decade of experience in the corporate and pharmaceutical industries. Successful Sarbanes Oxley compliance lead. Offering 3 years of experience in the Clinical Trials field also a Global Security Analyst offering more than 15 years of extensive experience with a unique combination of technical skills, and customer service excellence. Support ...
Tags for this Online Resume: SAP, Asset Management, Customer Relationship Management, Inventory, Lotus, Lotus Notes, Management, Microsoft Outlook, Microsoft SMS, it jobs, Service Now, OKTA, AD, Microsoft Office 365, Engaged IT, Technical Support, Client Services, IAM, Identity and Access Management
statistical programmer
As a certified SAS advanced programmer and SAS Clinical Trials Programmer, I am looking for a statistical programmer position in the pharmaceutical industry or health care field. I am hold green card.
Tags for this Online Resume: HIV, Oncology, Drug Screen, ELISA, Inventory, Microsoft Excel, Acquired Immune Deficiency Syndrome (AIDS), Ad hoc analysis, Data Analysis, Data Management, sql, javascript, html, statistical SAS programmer
Clinical Research - 20 Years of Experience - Near 91801
I have more than 25 years working in Research Clinical Trials. Diligent, civility skill, bilingual Spanish/English, Phlebotomy certified, and a great team player. Work as well with little or no supervision. Hours are flexible to meet jobs needs.
Tags for this Online Resume: clinical, phase i, phase iii, phase ii, clinical trials, phase iv, research, Phlebotomy, Protocol, Research Coordinator
Microbiologist - 15 Years of Experience
SUMMARY OF ACCOMPLISHMENTS * Developed more than 6 novel PET tracers for cancer diagnosis and evaluated them in mouse tumor models. Received "Bench to bedside" NIH grant of $240,000 and translated one of the tracers into clinical trials * Studied human adrenocortical carcinoma cancer using various tissue samples analysis including immunohistochemistry and gene expression analysis * Identified the mechanisms involved in NK c...
Tags for this Online Resume: PET, Allergy, Infectious Diseases, Oncology, DS, ELISA, Therapy, Imaging, Research, Cancer, oncology, clinical, pharmaceutical, trial, Immunology, Immuno-Oncology, vaccine
Research Assistant
Tags for this Online Resume: research, clinical, clinical trials, pharmaceutical
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 Regional Monitoring
Accomplishments: * Compliance- Maintained compliance with regulatory standards. Ensuring site staff was trained and followed all guidelines set forth by the FDA. * Implementation-Implemented a new tracking system that resulted in improved query resolution. * Documentation-Ensured study sites followed ALCOA to ensure accuracy of through precise documentation. * Patient Safety-Ensured quality control through following ICH/GCP...
Tags for this Online Resume: Audit, Compliance, Data Quality, Documentation, Forth Programing Language, Good Clinical Practices, ICH, Management, Monitoring, Protocol
Clinical Operations Manager - 6 years experience - North Carolina
Tags for this Online Resume: clinical operations, Quality Assurance, clinical research, clinical trials, vendor management, Study Start-Up / Activation, In-House CRA, regulatory, pharmaceutical, cro, phase iii, phase i, phase ii, Manager
Biostatatician
Accomplishments * Complete more than 100 studies including phase I to phase IV. * In charge of 20 phase I and 4 phase III study NDA submission tasks to ensure high quality deliverables that comply regulatory electronic submission guidance * Preparation of statistical analysis plans including mock up tables * Application of statistical section of clinical trial reports * Review of protocols/case report forms/statistical anal...
Tags for this Online Resume: SAS, Statistical Analysis, Documentation, Management, Pharmaceutical, Quality, Quality Assurance, Quality Control, Batch Processing, Biomedical Industry
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
In Between - 5 Years of Experience - Near 500081
Career Summary * SAS Certified Base for SAS9 with more than four years of experience. * Worked on different Phases of clinical trials and I have experience in programming, SDTM, ADAM and reporting in Clinical Research using SAS environments. As a Clinical SAS * Worked on Various Complicated SDTM domains like LB, MO & OE for ophthalmoscopy studies * Understanding of the study Documents and Data (e.g. Study design and objecti...
Tags for this Online Resume: A SERIES, Active Directory Application Mode (ADAM), Base SAS, Cardiology, Clinical Research, Data Management, Documentation, Generate Reports, HyperText Markup Language, Macro (Predefined Code)
