Contract SAS Programmer

Proclinical is currently recruiting for a SAS Programmer with a leading pharmaceutical company located in Princeton, NJ. As the SAS Programmer, you will be responsible for leading the statistical programming activities within the company.

Job Responsibilities:

• Participating in project team meetings to ensure timelines are met with high quality
• Performing quality control of SDTMs to ensure submission requirements are met.
• Create and be able to perform quality control of ADaMs to ensure submission requirements are met
• Performing quality control of ISE/ISS datasets, tables, figures and listings with quality within the timeline.
• Communicating effectively internally with the project team members and externally with various vendors.
• Performing ad-hoc analyses for in-house request or QC of such analyses under tight timelines
• Support database build and other data management programming activities
• Leading effort in building in-house programming tools and macros
• Reports to the Associate Director, SAS Programming

Skills and Requirements:

• Minimum educational experience is a BS in computer science, mathematics, statistics or related analytic field.
• Preferred educational experience is a Master's degree in Statistics/Biostatistics in the biopharmaceutical industry, with knowledge of biomedical sciences
• Minimum of 5-6 years of SAS programming and application development experience in pharmaceutical/biotech company
• Thorough knowledge of functional areas within the clinical development organization including but not limited to clinical operations, data management, statistics, medical writing and regulatory affairs.
• Deep understanding of the statistics/data management role in the broader clinical development setting
• Solid, hands-on knowledge of the use of statistical software (e.g., SAS or SAS Jump including SAS/GRAPH, and SAS/STAT), including report generation is necessary.
• Prior work experience in the CDISC SDTMs and ADaMs is a must.
• Prior experience in electronic NDA/BLA submissions via eCTD and responding to FDA/regulatory requests
• Strong MS Office skills (Word, Excel, PowerPoint), and skills in generating graphs and figures.
• Excellent verbal and written communication and interpersonal skills.
• Demonstrated ability to work in a team environment.
• High degree of motivation; results oriented.

If you are having difficulty in applying or if you have any questions, please contact Felix Hook at (+1) 646-367-2617 or f.hook@proclinical.com.

Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

Proclinical Staffing is an equal opportunity employer.

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