Description
Contract SAS ProgrammerTop Pharmaceutical Company
Onsite at Central New Jersey
2 year contract
Rate is open
Summary:
- Build programming specifications for safety and efficacy analysis database based on the Statistical Analysis Plan and report specifications (development of CDISC ADaM and SDTM)
-Create table shells for statistical analysis plans
- Generate analysis datasets, tables, listings and figures
- Generate all necessary output for the compilation of statistical appendices for reports
- Perform verifications of analysis datasets and tables, listings and figures created by another team member
- Complete programming projects on time and with the best quality control.
- Review and provide feedback on CRFs and edit specifications
Requirements:
- BSc in Mathematical, Statistical, Computer Science or Life Science. Masters preferred.
- 4-7 years of experience in Statistical Programming within Clinical Trials
- Extensive SAS programming experience
- Experience in CDSIC standards
** Must be onsite in Central New Jersey and able to Interview onsite this Friday 18th April for 1 hour.
Extremely Quick Process - Please send me updated resume today and let me know your availability for Friday Afternoon.
Thanks
Paul
To find out more about Real please visit www.realstaffing.com