SAS/Statistical Programmer 兼职 工作时间以外 北京

shiyiming

email: <!-- e --><a href="mailto:raynomad008@yahoo.com">raynomad008@yahoo.com</a><!-- e -->


Duties: Responsible for statistical programming in support (analysis datasets, pooled
datasets, listing and tables) of individual phase I-IV clinical trials and project
level activities for drug project / indications. Maintain efficient interfaces with
internal and external customers with support of SR management and the statisticians.
Develop and comply with project/study programming standards and specifications
following internal guidelines. Make certain that study documents and specifications are
consistent and comply with company standards by providing input into Study protocol,
CRF and Data structures and outputs (listings, tables and figures) for phase I – IV
clinical trials and submission activities.
Program according to specifications, analysis datasets, pooled datasets, listings,
tables and figures for phase I-IV clinical trials and for SCS and SCE with high quality
and within milestones.
Develop programming specifications for analysis datasets, pooled datasets and
deliverables in consultation with the statistician. Support quality control and quality
audit of deliverables.
Skills: Ability to coordinate programming work across a clinical study.
Experience in Oncology therapeutic area is a plus
Intermediate to expert knowledge of / experience with SAS software (including SAS macro
language) Working knowledge of database design/structures
Good understanding of global clinical trial practices, procedures and methodologies.
Education: BA/BS or equivalent experience in mathematics, statistics, computer
science, life sciences or related field, with at least 3 years of experience in a
programming role supporting clinical trials in the pharmaceutical industry, or MS
statistics/computer science with at least 2 years of similar experiences.