Biomedical Statistical Consulting® is looking for an incredible SAS/R Programmer to join our company and support our mission of providing best-in-class statistical services to our clients and partners. We are passionate about delivering high value and assisting Sponsors' statistical needs in Regulatory Clinical Trials.

A critical step in securing FDA approval of a drug or medical device is conducting a series of clinical trials capable of demonstrating safety and effectiveness. We specialize in designing these trials, using traditional methods and innovative novel approaches such as Propensity Score Matching, adaptive clinical trial design, and Bayesian design, to save costs, work around limited access to new data, and reduce bias in non-randomized studies.

SAS/R Programmer Purpose

We are looking for a passionate and experienced SAS/R Programmer to join our team! SAS/R Programmer are responsible for transforming raw clinical trial data into analyzing datasets, providing Tables, Listings, and Figures (TLFs), and maintaining and improving analysis algorithms and processes. This job will entail close collaboration with BSC™ Team members, as well as Regulatory and Clinical partners. High-quality clinical trial analyses and presentation are crucial for better decision-making.

Essential Duties

  • Process Electronic Data Capture (EDC) data into analytical datasets

  • Create Tables, Listings, and Figures to support Regulatory Clinical Trials

  • Develop and maintain SAS programs for data importing, quality assurance, and reporting.

  • Produce Define XML/PDFs, aCRFs, and Reviewers Guides to support SDTMs and ADaMs

Education and Experience

  • BS in Statistics, Computer Science, Mathematics, or a similar field. Work experience will be considered.

  • Deep knowledge of SAS. Skills in R and Python are a plus.

  • Programming experience in the CRO or Pharmaceutical industry

Required Knowledge Skills and Abilities

  • Knowledge of data standards for clinical research and statistical analysis (e.g., CDISC, SDTM, ADaM, ICH Statistical Principles for Clinical Trials)

  • Excellent oral and written communication skills

  • Ability to read, analyze, and interpret complex documents.

  • Strong organizational skills and flexibility to respond to changing deadlines.

Working Conditions/Physical Demands

While performing the duties of this job, the employee must be able to :

  • Maintain an excellent work ethic and the willingness to work additional hours as needed.  

  • Travel occasionally.  

  • Perform light work – exerting up to 20 pounds of force occasionally and/or a negligible amount of force frequently or constantly to lift, carry, push, pull or otherwise move objects.     

  • See, hear, talk and perform tasks requiring manual dexterity and visual acuity; kneel, sit, stand, walk, crouch, stoop, reach, pull, push and other similar, repetitive tasks requiring physical activity.   

  • Operate standard office/computer equipment.  

Equal Opportunity Employer

The Company is an equal opportunity employer. We value a diverse workforce and an inclusive culture. We encourage applications from all qualified individuals and do not discriminate, and will not tolerate discrimination, on the basis of race, ethnicity, color, religion, sex, pregnancy, gender, gender identity or expression, national origin, sexual orientation, age, national origin or ancestry, genetic information, political affiliation, physical or mental disability, military or veteran status, or any other protected status under federal, state or local law.  Our employment decisions are solely made according to qualifications for the positions.