Contract Clinical SAS Programmer - Pennsylvania

Clinical SAS Programmer12 month contractMust be onsite near Philadelphia, PAMid Size CRO
Responsibilities: - Build programming specifications for safety and efficacy analysis database based on the Statistical Analysis Plan and report specifications (development of CDISC ADaM and SDTM)

- Generate analysis datasets, tables, listings and figures to support writing of Clinical Study Reports and other regulatory filings
- Generate all necessary output for the compilation of statistical appendices for reports (e.g. Annual Safety Reports, Clinical Study Reports, Statistical Reports, etc)
- 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: - B.S/B.A or equivalent experience in computer science, mathematics, statistics, life sciences, or related field(s). M.S. in Statistics is a plus. - Proficient SAS programming skill with 3-5 years of experience working with clinical trial data. - Good understanding of clinical trial practices, procedures and methodologies. - Good verbal and written communication skills. - Good interpersonal and organizational skills. - Attention to detail and correctness. Please email or call me for more details. APPLY TODAY OR REFER A FRIEND. These are new openings at the moment and interviews are happening! Contact details are on my Linkedin. Search for Paul Dai at Real Staffing Group. ThanksPaul Dai
To find out more about Real please visit www.realstaffing.com