Clinical research jobs Clinical Research Associate Full-time Job

SAS Base & Macros #statistical #inferentialstatistics #statisticians #statistics #stat #probability #statisticsandprobability #statslove #statlove #mathematics #inferential #statistic #statsforlife #biostatisticians #statsforlifee #estimation #significance #inference #nonparametric #parametric #datascience #bigdata #analytics #interpretation #testing Job Description About Accenture: Accenture is a leading global professional services company, providing a broad range of services in strategy and consulting, interactive, technology and operations, with digital capabilities across all of these services. We combine unmatched experience and specialized capabilities across more than 40 industries powered by the world s largest network of Advanced Technology and Intelligent Operations centers. With 506,000 people serving clients in more than 120 countries, Accenture brings continuous innovation to help clients improve their performance and create lasting value across their enterprises. clinical research organization Visit us at www.accenture.com clinical research Project Role :Application Developer Project Role Description :Design, build and configure applications to meet business process and application requirements. Must Have Skills :No Technology Specialization,SAS Base & Macros Good To Have Skills : clinical  india placements Job Requirements : Key Responsibilities : CRITICAL Demand Some experience with Clinical data would be helpful Basic knowledge of Unix Import and Export Raw Data SAS programmers import and export raw data to add information to and extract information from various databases Manage Databases Create Data Sets and Programs Write Macros Analyze Data Write Reports Technical Experience : SAS Base Macros Professional Attributes : Good communication skills clinical research associates Educational Qualification : Degree Qualifications 15 years of full time educationReviewing data and identifying errors/inconsistencies The Trainee Clinical Data Coordinator maintains essential study documents for clinical research studies and enters data onto Case Report Forms and ensures study compliance. Prepares reports and assists with statistical analysis. Records accurate data by completing a paper or electronic CRFs.  sas in clinical research Under the Clinical Data Management Process tasks are assigned to Develop and maintain study-specific documentation, including Data Management Plans, eCRF specifications, CRF Completion Guidelines, Data Validation Guidelines, add Data Transfer Specifications, Coding Guidelines, Post Production Database Change Control Documentation, Database Audit, and Lock Procedures Perform and document database and report UAT Receive, integrate, and reconcile electronic data