Senior SAS Programmer

Advanced Clinical is a clinical development and strategic resourcing organization committed to providing a better clinical experience across the drug development journey. Our goal is to improve the lives of all those touched by clinical research – approaching each opportunity with foresight, character, resilience and innovation. Based on decades of experience, we help our clients achieve better outcomes by conducting candid conversations and anticipating potential issues through our customized solutions.
The Senior Statistical Programmer (“Programmer”) will have experience in all required areas of a Statistical Programmer II. The Senior Statistical Programmer is responsible for providing programming support for clinical trials.

Exceed expectations and responsibilities of a Statistical Programmer II
Understand and implement CDISC and other regulatory standards
Follow internal SAS programming conventions
Serve as programming lead on assigned studies
Create and maintain project timelines
Support the development of tools and macros to improve quality and efficiency of processes
Prepare programming specifications for SDTM, ADaM and other derived datasets
Apply knowledge of SAS programming to program/develop and/or validate statistical outputs according to the statistical analysis plan and other specifications; Analysis datasets (SDTM, ADaM, other derived datasets)
xml/Reviewer’s Guide
Perform ad hoc analyses of current and legacy databases
Work effectively with other programmers, statisticians, data managers, database programmers and other cross-functional team members to ensure accurate and high-quality statistical outputs
RFI completion, proposal development, bid defense participation, attendance at industry/scientific meetings, etc.

May assist in the preparation and review of monthly financial reporting
The ideal candidate should have a degree in Statistics, Computer Science, or a closely related field; work experience may be substituted for degree
Minimum of 4 years direct SAS programming experience in pharmaceutical development or CRO environment
Good knowledge of medical terminology and conduct and analysis of clinical trials
Knowledge of relevant industry data standards (e.g. At Advanced Clinical, our commitment to diversity and inclusion in every part of our organization is crucial to fulfilling our mission and demonstrating our REAL values. Diversity thereby strengthens the legitimacy and relevance of Advanced Clinical in delivering services to our clients. We seek talented, creative individuals from a variety of backgrounds and cultures to work with us. It is our priority that our workplace be inclusive, welcoming of diverse ideas and appreciative of valuable experience.

It is Advanced Clinical’s practice not to discriminate against any Employee or applicant because of sex, race, color, age, national origin, religion, gender, gender identity or expression, sexual orientation or sexual preference, pregnancy or maternity, genetic information, marital status, physical or mental disability, medical condition, military or veteran status, or any other basis protected by applicable federal, state, or local law.

This practice applies to all terms and conditions of employment including, but not limited to, hiring, training, compensation, benefits, promotions, transfers, layoff, Company-sponsored education, social and recreational programs, and treatment on the job. If you have a disability or handicap and would like us to accommodate you in any reasonable way, please inform your Recruiter so that we can meet to discuss the appropriate alternatives available.

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