Contract Opportunities: North America
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0000105271-Contract SAS Programmer6693
State: NJ
Job Description:

• Provide programming input to CRF, SAP, analysis file specifications, and tables, figures, and listings (TFLs) shells.
• Write SAS programs to generate derived analysis datasets, perform analysis, and TFLs.
• Perform ad hoc flexible and rapid programming arising from questions generated from planned analyses and results.
• Perform programming validation to ensure quality of analysis datasets and programming outputs.
• Provide input to the design of the clinical trial database for proper data capture and to ensure data quality.
• Create Data Definition Tables (DDT) and convert TFLs to the required format for eSubmission.
• Provide programming support for the preparation of integrated reports, submissions and post-submission activities.
• Convert, verify and integrate multiple sources of incoming data for the creation of analysis datasets.
• Serve as a coordinator when multiple programming resources (e.g. CROs or contractors) are used.
• Contribute to the creation, maintenance, and validation of standards for outputs and macros.

Skills/Knowledge Required:

• Bachelor’s degree in life science, statistics, mathematics, computer science, or related field required; Master’s degree is preferred.
• 5 plus years Pharmaceutical/CRO experience as a SAS programmer supporting clinical trials for regulatory submissions.
• Demonstrated proficiency in using SAS to produce derived analysis datasets and TFLs.
• Have in-depth understanding of clinical data structure and relational database.
• Demonstrated skills in using software tools and applications, e.g., MS office, XML.
• Demonstrated ability in the handling and processing of upstream data, e.g., multiple data forms, workflow, eDC, SDTM.
• Demonstrated ability in providing outputs to meet downstream requirements, e.g., ADaM, Data Definition Table, e-submission.
• Have in-depth understanding of regulatory, industry, and technology standards and requirements.
• Have good knowledge of statistical terminology, clinical tests, medical terminology and protocol designs.
• Demonstrated ability to work in a team environment with clinical team members.

Please send your resume to
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Syneos Health US, Inc. is an Equal Opportunity Employer, M/F/Disabled/Vets that values the strength that diversity brings to the workplace.