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Online Resumes with "crf"
Clinical Research - 9 Years of Experience - Near 45999
- 3 clinical research studies while developing an understanding of the drug development process Good Clinical Practices and relevant regulations. Perform management of study site activities to ensure the integrity of clinical data in adherence to all applicable regulatory guidelines and Standard Operating Procedures (SOPs). New experience oncology trials (lung cancer melanoma antigen-specific immune-therapeutics) RDE (elect...
Tags for this Online Resume: Clinical Research, Research, Oncology, Overdose, Cord Injury, SAP MM module, Application Support, Good Clinical Practices, Management, Support
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)
Programmer Analyst
SUMMARY * 6 years of experience as a Statistical Programmer in Clinical trials of Pharma Industry. * Expertise in SAS programming features like BASE SAS, SAS/MACROS, SAS/STAT, SAS/GRAPH, SAS/SQL, and ODS. * Skilled in generating reports featuring various SAS procedures, like Proc Report, Proc Summary, Proc Freq, Proc Mean, Proc Transpose, Proc sort, Proc Univariate, Proc Datasets, Proc Compare, Prco SGPLOT, and Proc SQL. * ...
Tags for this Online Resume: Base SAS, Macro (Predefined Code), Proc, SAS, SAS/STAT, Statistical Analysis, Structured Query Language, Data Analysis, HyperText Markup Language, Microsoft Excel
Quality Coordinator
Professional Summary: * Certified clinical research professional with nearly 10 years of clinical research experience in the medical device industry. I have a wide range of knowledge with site and study management having worked as an In-house/Field CRA, Lead CRA and Clinical Trial Assistant. * Conducting: Qualification, Initiation and Close-Out monitoring visits for pre and post-market trials. * Start-up activities for both...
Tags for this Online Resume: Documentation, Management, Data Management, Budgeting, Clinical Operations, Clinical Research, Collection, Compliance, Contract Negotiations, Distribution
Clinical Research - 1 Years of Experience - Near 60091
Leverage Masters and Medical Degrees in clinical trials for new drugs and medical devices.
Tags for this Online Resume: AMICUS, Phlebotomy, Medical, Research, Cancer, clinical trials, regulatory, phase iii, phase ii, pharmaceutical, IRB, eCRF, Rave, ICF, Clinical Protocol, IB, Apheresis, Hematology, Leukemia Trials, GCP, Human Subject Protection, Medicine, HIPPA, Responsible Conduct of Research
Documentation Associaye 17 years Experience in Pharmaceutical industry
CAREER SUMMARY Quality Assurance Professional with experience in pharmaceutical manufacturing enforcing quality standards in a manufacturing unit. Skilled at studying industry and consumer requirements, running tests, writing quality assurance procedures, preparing quality reports, and assigning quality assurance tasks to employees. Proficient interacting with various departments including Supply Chain, Production, MS&T, Va...
Tags for this Online Resume: Documentum, Documentum (Wkflow Sw), Supply Chain, Change Control, Compliance, Corrective Actions, Documentation, Folder, Forecast, Management
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
Database Designer
Summary: My most recent work experience was performing data conversion from customer-provided source data to a target Fleet Management database and Web page configuration on the application. I have also worked in the past as a C/C++ developer as well as working on designing logic flow on Electronic Diaries for Clinical Trials. I have a recognized skill in understanding new platforms and systems as well as an expertise in pr...
Tags for this Online Resume: Management, Application Development, Billing, Data Conversion, Data Mapping, Database, Fleet Management, HyperText Markup Language, Irix, Javascript
Clinical Research - 8 Years of Experience
PROFESSIONAL SUMMARY Nearly 8 years of Industry experience with efficient skillset in Operations, Project Management (Clinical Data Management). Possess strong analytical & management skills. Extensive knowledge in Study set-up and Delivery Management, Process improvement. Working experience in managing top pharma sponsors. Managed high revenue generated studies during the tenure. My core beliefs are integrity and honesty a...
Tags for this Online Resume: Data Management, Management, Adobe, Audit, Business Development, Cardiovascular, Coding, Data Manager, Database, Database Design
Clinical Review, RN: Chapel Hill, NC
To make sure all that project, federal,and company specific guidelines are followed by personel connected to the study (patient) to ensure patient safety and accurate data.
Tags for this Online Resume: RN , review, CRF, CRA, legal, case
Accountant
Tags for this Online Resume: Accounting, Financial, Financial Services, Retail, Services, Accounting Software, Bank Deposits, Bank Reconciliation, Cash Management, Deposits
Licensed Nurse - 20 Years of Experience - Near 18974
I have extensive experience in writing clinical and regulatory documents in the Pharmaceutical industry which include regulatory and safety I have completed medical encoding (MeDRA), data and quality review management. My past experience included responsibilities for preparing safety sections within key documents such as Investigations Brochure, clinical study reports, writing safety narratives to be included in final stud...
Tags for this Online Resume: Management, Oncology, DS, Query, Medical, Oracle, Oracle Clinical, Database, Encoder, Risk Management
