Statistical Programmer (OnSite)

Our client located in Waltham, MA is seeking a Statistical Programmer to join their team on a long term contract looking to last 12 Months. This individual must be available to be onsite for the duration of the project.

Key Responsibilities:

• Does both production and QC programming of SDTM datasets, analysis datasets, tables, listings, and figures, for multiple clinical trials using SAS software.
• Ensures standards at a drug program level; integrates data across multiple studies or drug programs.
• Works with minimal supervision under the direction of a lead programmer.
• Communicates issues to lead programmer or manager.
• Must meet timelines or communicate proactively and effectively if timelines are at risk so that plans can be adjusted.
• Expected to contribute to departmental process improvement initiatives.

Essential Skills and Qualifications Required

• Must have strong time management and communication skills.
• Able to handle a moderate to large volume of complex tasks with minimal supervision.
• Able to handle ad-hoc requests with minimal guidance.
• Recognizes when negotiating skills are needed and seeks assistance when necessary.
• Excellent organizational, interpersonal, and communication skills.
• Previous SAS programming experience, including SAS STAT, GRAPH and MACRO.
• Previous relevant pharmaceutical/biotech industry experience.
• Extensive knowledge of drug development process and clinical trials.
• Extensive knowledge of drug submission requirements, relevant ICH and FDA/EMEA guidelines, CDISC standards.

Education and Experience Requirements

• Bachelor's degree or equivalent, preferably in a scientific discipline such as Statistics, Mathematics, Economics, Computer Science, IT, Biology, Social Science, etc.
• 3 to 10 years of pharmaceutical/biotech industry experience.

Sthree US is acting as an Employment Business in relation to this vacancy.