*Hello,* *This is Sandeep from Neumeric Technologies..*
*Please go through the following requirement and also if interested, please fill the details below..* *Please send the resumes to [email protected]* *SAS Developer** New London, CT 6+ months* · Create submission-ready standard data presentations and data sets using standard coding and following standard industry processes including SDLC · Creating SAS programs and producing outputs to support the analysis and reporting of clinical trials. · Developing analysis datasets for trial level reporting by following the Analysis Data Model (ADaM). Programming standard and custom data listings, summary tables, and graphs as specified in statistical analysis plan · Extract the data from clinical database for data reporting purpose. · Develop programming specifications by analyzing the protocol related documents. Meet the programming requirements for submissions as required · Understand and plan work to delivery timelines including allowing time for internal QC, as appropriate · Whenever required, collaborate with the statistician, data managers, and clinicians to resolve specifications and data related issues. · Work with supervisor to balance conflicting priorities · Understand timelines for and milestones affecting their work and alert supervisor and client representative to potential slippage · Run routine QC programs, track the changes in programming and specifications, and document the QC results and resolutions. · Carry out rework as requested by supervisor or client representative · Follow escalation process and neither suppress nor over- escalate issues Contribute to close –out evaluations and any discussion · Other duties as assigned. * Professional/Technical Skills & Experience* · Experience of extracting, manipulating, summarizing, analyzing and presenting data using SAS procedures · Experience of SAS programming, Macro development, SQL and SAS/Connect procedures. · Strong knowledge of reporting procedures like proc report, proc summary, and proc tabulate. · Strong knowledge of SAS/GRAPH and Statistical procedures related to SAS/STAT · Ability to validate SAS programs that produce derived-analysis datasets and data analyses · Some experience in preparations for NDA filings. Thorough understanding of regulatory guidelines like · Good Clinical Practices (GCP), ICH guidelines, 21 CFR part-11 compliance requirements. · Knowledge of coding dictionaries (WHO, COSTART, ICD-9, MedDRA) expected · Knowledge of CDISC® related data models like SDTM, and ADAM. · Proficiency in Microsoft Office Applications · Excellent verbal and written communication skills · Detail oriented, ability to multitask with strong prioritization, planning and organization skills · Excellent team player · *Key Skills:* SAS Clinical CDISC Macro development *If your are comfort, please fill all the below details !!!* * * *Full Name: * *Email:* *Phone:* *Visa:* *Availability:* *Relocation:* *Current location:* *Skype ID:* Best Regards, *Sandeep* *Neumeric Technologies*** Visit us at www.ntc-us.com for further details Work: 614 504 8804 Email: [email protected] Yahoo: sandeep_abcd567 *Oracle Gold Partner | Microsoft Partner | IBM Partner* *-- Ask us about our $500 referral fees/incentive policy --* ___________________________________________ Disclaimer: This email and any files transmitted with it are confidential and intended solely for the use of the individual or entity to whom they are addressed and do not constitute a commitment by Neumeric Technologies Corporation, USA except where provided for in a written agreement between you and the Company. If you are not the intended recipient of this message, delete it and notify sender immediately. Please check for viruses before opening attachment. * * -- You received this message because you are subscribed to the Google Groups "Citrix and Sap problems" group. To unsubscribe from this group and stop receiving emails from it, send an email to [email protected]. To post to this group, send email to [email protected]. Visit this group at http://groups.google.com/group/citrix-and-sap-problems. For more options, visit https://groups.google.com/groups/opt_out.
