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Pharmaceutical Research Associates, Inc. Senior Statistical Programmer I in Blue Bell, Pennsylvania

Pharmaceutical Research Associates, Inc. seeks a Senior Statistical Programmer I in Blue Bell, PA.

 

Duties:

• Deliver high quality SAS programming outputs for all assignments that consistently meet study timelines, quality standards, sponsor and/or contractual requirements.

• Lead programming deliverables for assigned studies, including implementation of resource planning, tracking, work allocation and quality control of junior level programmer deliverables

as deemed appropriate to level.

• Keep management informed of project status in relation to quality, timelines and/or performance issues.

• Adhere to programming specifications and study specific requirements, including completion and filing of required documentation.

• Efficient use of SAS, and adherence to SAS programming guidelines.

• Create listing and safety outputs (analysis datasets. tables, figures) to a high standard of quality and accuracy.

• Validate listing and safety outputs (analysis datasets, tables, figures) per departmental procedures.

• Create efficacy outputs (analysis datasets, tables, figures) to a high standard of quality and accuracy.

• Validate efficacy outputs (analysis datasets, tables, figures) per departmental procedures.

• Create complex programs (such as project or departmental macros) to a high standard of quality and accuracy.

• Liaise effectively with other ICON functions (e.Q., DMPM, MW), as required during the life of the project.

• Learn, share, and apply new techniques and technologies to increase efficiency and to implement industry trend solutions (e.g., SDTM, ADaM).

 

Requires a Bachelor's degree in a Computer Science, Statistics, or Mathematics or scientific field plus six (6) years of experience

in the following:

• Programs statistical analyses (via analysis datasets, tables, figures, listings, etc.) using an Appropriate statistical analysis software tool (e.g., SAS®), and may include tabulation datasets.

• Acts as a key member of the project team by attending team meetings and working with biostatisticians, data managers and project managers.

• Performs programming using techniques such as macro language, advanced data manipulation, and statistical procedures.

• Demonstrates a good understanding of analysis data structure standards (ADaM) and if applicable, tabulation data structure standards (SDTM).

• Contributes to departmental initiatives and acts as an SME on technical subjects as applicable.

• Applies leadership skills in the coordination clinical study programming activities and projects.

• Undertakes analysis and investigation to identify and define problems. Anticipates future issues. Work is done independently, reviewed at critical points.

Telecommuting is permitted.

 

Must also have authority to work permanently in the U.S. Applicants who are interested in this position may apply https://www.jobpostingtoday.com/ Ref # 49254

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