-- *Please send reply to [email protected] * *-All our requirements are Direct client Requirements.* *-Please share the resumes only after you discuss with your consultant.* *-Resumes with Linkedin URL / 2 Professional references only will be processed.*
Role: Sr. Clinical SAS Programmer Location: Canton, MI Duration: 1 to 3 Years Required Skills: Strong programming and logic skills Hands-on with clinical trials and pharmaceutical development 8+ years SAS programming, SAS Base, SAS Macro and thorough knowledge of clinical database structures Ability to program data presentations, using programs such as SAS procedures Sound experience with data and production of TLGs Previous hands-on experience with CDISC and ADaM are essential prerequisites Experience in table and CDISC validation Attention to detail and data mining as needed for data review Experience in the pharmaceutical or CRO industry is preferred. Excellent organizational and communication skills are require Thanks & Regards, *Mohan Ganti* Mail: [email protected] *Disclaimer: We respect your Online Privacy. This is not an unsolicited mail. Under Bill 1618 Title III passed by the 105th U.S. Congress this mail cannot be considered Spam as long as we include Contact Information and a method to be removed from our mailing list. If you are not interested in receiving our emails then please reply with a "REMOVE" in the subject line and mention all the email addresses to be removed with any email addresses.* -- You received this message because you are subscribed to the Google Groups "SAP BASIS" 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/sap-basis. For more options, visit https://groups.google.com/d/optout.
