Multiple Positions: Senor SAS- Statistical Programmer-Clinical, Durham, NC
Hi Partners, Hope you are doing well. Please let us know if you have anyone for below mentioned positions with resume and following details of your consultant Full Name/Phone/Email/Current Location/Availability/Rate Reply at *sat...@canbayinc.com sat...@canbayinc.com* and * n...@canbayinc.com n...@canbayinc.com* for quick response *Position: **Senor Statistical Programmer (Clinical)* *Location: Raleigh/Durham, NC* *Duration: Length: 6 months, possibly renewable* *No. of Positions: Multiple* *Job Description* The Senor Statistical Programmer provides technical expertise for the conduct of clinical trials, might act as an internal subject matter expert in specific areas providing technical support and expert advice, and works independently to support various programming activities related to analysis and reporting. • Coordinate project start-up activities, including Unix/PMED project area set-up, creation of global programs (e.g., set-up SAS, format SAS, etc.), tracking spreadsheets, and required documentation. • Assist in the production and QC of analysis plans, TLF mock-shell development, derived dataset specifications, programming specifications, and other process supporting documents. • Use efficient programming techniques to produce and/or QC derived datasets tables, figures and data listings. • Understand regulatory requirements concerning industry technical standards (e.g., CDISC, 21 CFR Part 11, electronic submissions, etc.) and implications for the department. • Provide input into monthly PERFORM forecasts and monitor the completion of forecasted units. • Create standard macros and applications to improve the efficiency of the department. **Job Qualifications* • Minimum of 5 years’ industry experience • Strong technical skills required – specifically around Macro standardization and infrastructure build-out. • Proficiency in SAS • First degree (undergraduate or equivalent) in a relevant discipline is preferred or equivalent work experience. • Excellent English written and oral communication skills. • Relevant Clinical Trial industry experience *Please contact my manager Satish Saini for more details for these open position at his number 732-230-4327 or email: sat...@canbayinc.com sat...@canbayinc.com * *Thanks Regards,* *Nitu Bansal * *Canbay Technology Solutions, Website: www.canbaytech.com http://www.canbaytech.com* *100 Jersey Avenue, Suite A 103, New Brunswick, NJ 08901* *Fax: 973 577 6989* *Email: n...@canbayinc.com n...@canbayinc.com* -- You received this message because you are subscribed to the Google Groups SAP ABAP group. To unsubscribe from this group and stop receiving emails from it, send an email to sap-abap+unsubscr...@googlegroups.com. To post to this group, send email to sap-abap@googlegroups.com. Visit this group at http://groups.google.com/group/sap-abap. For more options, visit https://groups.google.com/d/optout.
Multiple Positions: Senor SAS- Statistical Programmer-Clinical, Durham, NC
Hi Partners, Hope you are doing well. Please let us know if you have anyone for below mentioned positions with resume and following details of your consultant Full Name/Phone/Email/Current Location/Availability/Rate Reply at *sat...@canbayinc.com sat...@canbayinc.com* and * n...@canbayinc.com n...@canbayinc.com* for quick response *Position: **Senor Statistical Programmer (Clinical)* *Location: Raleigh/Durham, NC* *Duration: Length: 6 months, possibly renewable* *No. of Positions: Multiple* *Job Description* The Senor Statistical Programmer provides technical expertise for the conduct of clinical trials, might act as an internal subject matter expert in specific areas providing technical support and expert advice, and works independently to support various programming activities related to analysis and reporting. • Coordinate project start-up activities, including Unix/PMED project area set-up, creation of global programs (e.g., set-up SAS, format SAS, etc.), tracking spreadsheets, and required documentation. • Assist in the production and QC of analysis plans, TLF mock-shell development, derived dataset specifications, programming specifications, and other process supporting documents. • Use efficient programming techniques to produce and/or QC derived datasets tables, figures and data listings. • Understand regulatory requirements concerning industry technical standards (e.g., CDISC, 21 CFR Part 11, electronic submissions, etc.) and implications for the department. • Provide input into monthly PERFORM forecasts and monitor the completion of forecasted units. • Create standard macros and applications to improve the efficiency of the department. **Job Qualifications* • Minimum of 5 years’ industry experience • Strong technical skills required – specifically around Macro standardization and infrastructure build-out. • Proficiency in SAS • First degree (undergraduate or equivalent) in a relevant discipline is preferred or equivalent work experience. • Excellent English written and oral communication skills. • Relevant Clinical Trial industry experience *Please contact my manager Satish Saini for more details for these open position at his number 732-230-4327 or email: sat...@canbayinc.com sat...@canbayinc.com * *Thanks Regards,* *Nitu Bansal * *Canbay Technology Solutions, Website: www.canbaytech.com http://www.canbaytech.com* *100 Jersey Avenue, Suite A 103, New Brunswick, NJ 08901* *Fax: 973 577 6989* *Email: n...@canbayinc.com n...@canbayinc.com* -- You received this message because you are subscribed to the Google Groups SAP ABAP group. To unsubscribe from this group and stop receiving emails from it, send an email to sap-abap+unsubscr...@googlegroups.com. To post to this group, send email to sap-abap@googlegroups.com. Visit this group at http://groups.google.com/group/sap-abap. For more options, visit https://groups.google.com/d/optout.
