Clinical SAS Programmer

Responsibilities:

Conduct clinical programming to support clinical data management, data cleaning, and data review, as well as external data reconciliation in accordance with standards (CDISC, MedDRA, WHO-DD, FDA)/SOPs or study specific guidelines

Work with Data Manager to generate and review database specification documents, CRF specifications, edit checks specifications and data management documents

Conduct clinical programming to create data sets, tables, figures, and listings for reports

Perform data checks, program/document validation as needed to ensure integrity and correctness of data

Support the development, delivery and maintenance of clinical data review standards, tools and systems

Responsible for documentation to support the programming and inspection

Perform other duties as assigned

Qualifications:

Bachelor’s degree or equivalent. Master’s degree in a scientific discipline such as Computer Science, Life Sciences, Statistics, etc. preferred.

Programming and analytical skills using SAS, R, Python or similar.

Excellent verbal and written communication skills

Able to work on multiple, concurrent projects

A high degree of accuracy and attention to detail

Knowledge of clinical trial study design a plus

Employment is subject to a background check

Full-Time