| Urgent Requirement || Sr. SAS Programmers || Remote || 3 Years at Remote, Remote, USA |
| Email: [email protected] |
| From: Suraj Prashar, Pivotal [email protected] Reply to: [email protected] Hi, Hope you are doing great!! Please find the requirement below, If you find yourself comfortable with the requirement please reply back with your updated resume and I will get back to you or I would really appreciate if you can give me a call back at my contact number (703) 570-8775 * (Ext. 232). Job Title: Sr. SAS Programmers Location: Remote Duration: 3 years Visa Type: NoH1/OPT/CPT Job Description:- Should have 100% experience in Clinical SAS (No financial SAS background) 6+ years, ideally 7-10 years overall experience (Must have 3+ years of US Based experience) Key Responsibilities Include but are not limited to: Provide quality deliverables by following corporate and departmental policies, procedures and applicable standards. Perform data manipulation, analysis and reporting of clinical trial data. Create analysis files, tables, listings, and figures and validation of those files. Maintain project tracking and validation documentation. Work well in an environment where team members may be distributed across multiple locations. Review planning documents (Statistical Analysis Plan, dataset specifications, etc.) to ensure project objective alignment, clarity, accuracy and completeness of programming requirements. Present statistical programming concepts to non-programming team members as necessary Collaborate effectively with cross-functional teams and interface with multiple stakeholders to manage timelines and priorities. Serve as back-up to Principle Statistical Programmer as needed. Basic Qualifications BA/BSc in Statistics, Mathematics, Computer Science, Life Sciences or other related scientific subject with at least 8 years of relevant experience or Masters degree and at least 6 years Prior regulatory submission and response experience Excellent analysis and reporting skills Command of drug development life cycle and experience with the manipulation, analysis and reporting of clinical trials data Knowledge of latest CDISC SDTM standards and familiar with CDISC ADaM and Define standards. Ability to work effectively and successfully in a dispersed team environment with cross-cultural partners. Excellent oral and written English communication skills. Excellent time management skills, able to meet required timelines. Ability to provide quality output and deliverables, in adherence with timelines. Willingness and ability to learn and follow standard processes and procedures. Preferred Qualifications Familiarity with other programming languages (e.g. Java, R, or S-Plus) In depth knowledge of SAS Graph and Stat packages Keywords: business analyst rlang |
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| Wed Sep 27 21:56:00 UTC 2023 |