programmer.

• Act as primary point of contact for all SAS programming activities.

• Plan programming deliverables.

• Oversee vendors’ programming deliverables.

• Develop SAS programs for SDTM, ADaM, Patient Profiles, Tables, Listings and Graphs of high complexity in support of Statistical Analysis Plan, posters, Integrated Summary of Safety (ISS) and Integrated Summary of Efficacy (ISE).

• Programming support for medical review listings and other activities need data summary and data mining.

• Drive programming activities to ensure quality and on-time deliverables. • Good experience with regulatory submission.

• Review draft and final production runs for project to ensure quality and consistency.

• Represent Statistical Programming during vendor audits ensuring study documentation is maintained and filed according to company processes.

• Carry out all activities according to company SOPs and to Good Clinical Practice (GCP).

• Demonstrate expertise in technical/programming skills.

• Demonstrate knowledge of clinical trials activities.

• Demonstrate leadership skill.

skills and experience required.

• Education: Bachelor’s degree or above in computer science, statistics, mathematics or other scientific field (or equivalent theoretical/technical depth).

• 5+ years of experience programming and analyzing in a pharmaceutical/clinical trial environment.

• Fluent in written and spoken English.

• Knowledge of clinical trials and statistical methodology.

• Advanced SAS skills, Macro programming and SAS/STAT.

• Knowledge of regulatory requirement on drug development procedure and CDISC.