*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 "CorptoCorp" 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/corptocorp. For more options, visit https://groups.google.com/groups/opt_out.
