| Urgent Need Clinical SAS || Remote at Remote, Remote, USA |
| Email: [email protected] |
| From: Renu Sharma, Vyze Inc. [email protected] Reply to: [email protected] Hi, I have a very urgent role. If interested then please send me your resume along with below information. Full Name: Visa: Email: Phone: Location: Relocation: Rate(C2C/1099): Skype Id: Start: Job Title: Clinical SAS Location: Remote Duration: 6 Work Authorization: GC/USC MOI: SKYPE We would be looking for 6 years of ClinicalSAS experience in the US. The Statistical ProgrammingContractor supports statistical programming activities in the production of theanalysis datasets, tables, listings, figures, electronic submission components,and complex ad hoc analyses. Depending on experience level, may lead a study. Responsibilities: Does both production and QC programming of SDTM datasets, analysis datasets,tables, listings, and figures, for multiple clinical trials using SAS software. Ensures standards at a drug program level; integrates data across multiplestudies or drug programs. Works with minimal supervision under the direction of a lead programmer. Communicates issues to lead programmer or manager. Must meet timelines or communicate proactively and effectively if timelinesare at risk so that plans can be adjusted. Expected to contribute to departmental process improvement initiatives. General Knowledge and Skills: Able to handle a moderate to large volume of complex tasks with minimalsupervision. Able to handle ad-hoc requests with minimal guidance. Recognizes when negotiating skills are needed and seeks assistance whennecessary. Excellent organizational, interpersonal, and communication skills. Minimum Educational and Experience Requirements: Bachelors degree or equivalent, preferably in a scientific discipline suchas Statistics, Mathematics, Economics, Computer Science, IT, Biology, SocialScience, etc. Previous SAS programming experience, including SAS STAT, GRAPH and MACRO. Previous relevant pharmaceutical/biotech industry experience. Extensive knowledge of drug development process and clinical trials. Extensive knowledge of drug submission requirements, relevant ICH andFDA/EMEA guidelines, CDISC standards. Open to all levels ranging from 3 to 10 years of pharmaceutical/biotechindustry experience Thanks & Regards.. Renu Sharma||Technical Recruiter Vyze Inc 24916 Earls Ford Drive Chantilly, VA 20152 Email: [email protected] Keywords: active directory information technology green card Idaho Virginia |
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| Sun Feb 05 01:37:00 UTC 2023 |