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This is very urgent opening. Please send your available matching candidates on ke...@riderconsultinginc.com I have wonderful opportunities for SAS Professionals. We have 4 locations NJ/MA/CA/ILbut we need candidates only with linked in profiles. Please share resumes only of the candidates who has an up to date linked in profile. Also mention that you are applying for which role and what location. Share your resumes accordingly. 1.Title: SAS Statistical Programmer Location: Boston MA Years of Experience: 7-10 Years Duration: 1.5 year contract Job Description The Statistical Programming Contractor supports statistical programming activities in the production of the analysis 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 multiple studies 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 timelines are 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 minimal supervision. • Able to handle ad-hoc requests with minimal guidance. • Recognizes when negotiating skills are needed and seeks assistance when necessary. • Excellent organizational, interpersonal, and communication skills. Minimum Educational and Experience Requirements: • Bachelor’s degree or equivalent, preferably in a scientific discipline such as Statistics, Mathematics, Economics, Computer Science, IT, Biology, Social Science, 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 and FDA/EMEA guidelines, CDISC standards. • Open to all levels ranging from 3 to 10 years of pharmaceutical/biotech industry experience 2.Title: Lead SAS Consultant Location: New Jersey Years of Experience: 7-10 Years Duration: 1 year contract Skills/Knowledge Required: • BA/BS degree in life science, statistics, mathematics, computer science, or related field OR equivalent working experience required. • 7-10 years Pharmaceutical/CRO experience as a SAS programmer supporting clinical trials for regulatory submissions. • Demonstrated knowledge in programming environments, systems and networking as it relates to the pharmaceutical industry. • Have in-depth understanding of clinical data structure as well as relational databases • Demonstrated proficiency in using SAS • Demonstrated skills in using software tools and applications, e.g., MS office, XML, HTML, etc. • Have an understanding of regulatory requirements pertaining to technology, systems, and standards. • Ability to research new technologies and ensure alignment with regulatory agencies and industry standards • Demonstrated ability in the handling and processing of upstream data, e.g., multiple data forms, workflow, eDC, SDTM. • Demonstrated ability in providing outputs to meet downstream requirements, e.g., ADaM, Data Definition Table, e-submission. • Demonstrated ability to work in a team environment with clinical team members. • Excellent planning and project management skills. • Good interpersonal, communication, writing and organizational skills. 3.Title: Sr. SAS Programmer Location: San Francisco & LA, CA Years of Experience: 8+ Years Length of Contract: 1 Year Desired skills and expertise: . Create SAS programs for data mining . Gather study team requirements and translate them into technical specifications for SAS programs . Program SAS data validation checks and listings to identify data discrepancies . Program SAS checks to integrate and reconcile data from external sources (including serious adverse events (SAE), lab results, ECGs, electronic patient records, medical devices and interactive voice response (IVR)) into the primary clinical database SAS datasets . Review Case Report Forms and formatting of SAS datasets extracts for accuracy and consistency . Provide programming support for Annual Safety Reports and Publications . Build standard SAS Macro library . Mentor junior level SAS programmers, if needed . MUST have prior FDA submission experience. . MUST have Oncology clinical trials . Bachelors Degree in related area . Minimum of 8+ years of SAS programming experience within the biotechnology/pharmaceutical industry . Familiarity with CDISC/ Study Data Tabulation Model (SDTM), ICH/GCP, 21 CFR 11 . Excellent SAS 9.2 programming skills . Familiarity with Data Management software (e.g. Medidata, Oracle Clinical) . Familiarity with coding dictionaries MeDDRA and WHODRUG . Possess excellent communication skills . Good organizational skills and ability to prioritize tasks . Must be able to work under tight timelines 4.Job Title: SAS Analytics Location: Vegas & Chicago, IL Years of Experience: 2 – 5 Years Length of Contract: 1 Year Desired skills and expertise: · Good hands-on expertise in SAS and SQL · Excellent presentation and communication skills. Prior client management experience preferred. · Willingness to learn and try new things proactively · Entrepreneurial in nature; self-motivated; work with minimal guidance · 2-5 years of relevant analytics experience, preferably from a consulting background · Valid US work permit Job responsibilities: · Perform complex data analysis in support of business growth · Help translate business problems to analytical frameworks; extract insights from consumer, sales and other data available and provide data analysis, synthesis & presentation support · Ensure all deliverables meet client expectations in terms of scope, speed & quality Thanks. KevinPatel Ph No:- 980-819-0687 E-mail:- ke...@riderconsultinginc.com G-Talk : kevinpatel.ri...@gmail.com Web Site :- www.riderconsultinginc.com -- You received this message because you are subscribed to the Google Groups "Citrix and Sap problems" group. 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