Convert legacy SAS datasets from 8-10 clinical studies into Clinical Data Interchange
Standards Consortium (CDISC) Study Data Tabulation Model (SDTM) datasets. This
position reports into the Associate Director, Data Management and Programming
and is estimated to last up to 1 year.
- Independently create SDTM specifications based on CDISC SDTM standards.
- Collaborate and review specifications with other programmers and biostatisticians
for consistency and accuracy among the studies.
- Program SDTM datasets from the raw datasets, according to the SDTM standards.
- Validate SDTM datasets with the raw datasets, and document the validation
results.
- Create the final Data Definition Table for each study.
- Create CDISC SDTM annotated CRFs.
- May review SDTM specifications produced by others.
- May develop specifications for non-standard data.
- A minimum of 5 years of SAS programming experience in biotech/pharmaceutical
industry.
- B.S. degree in Computer Science, Statistics, or related field required.
Master's degree in Statistics is a plus.
- Proven experience in programming CDISC SDTM datasets and Data Definition
Tables (DDT) is essential.
- Good communication skills (verbal and written).
- Able to collaborate effectively with the team to meet project timelines.
- Must be able to work independently.
Affymax, Inc.
Human Resources
4001 Miranda Avenue
Palo Alto, CA 94304
careers@affymax.com
