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Current Opportunities

Department: Clinical Operations

Job Title: Senior Clinical Statistical Programmer

Location: Andover, MA

Report To: Executive Director, Biostatistics

TransMedics, Inc., is the world’s leader in portable ex-vivo warm perfusion and assessment of donor organs for transplantation. Headquartered in Andover, Massachusetts, the company was founded to address the unmet need for more and better organs for transplantation, and has developed technologies to improve organ quality, validate organ viability, and increase the utilization of transplant organs for the treatment of end-stage heart, lung, and liver failure. We are currently hiring a Senior Clinical SAS Programmer at our Andover, MA headquarters to help revolutionize transplant medicine. This is a hands-on role in a fast-paced and dynamic medical device company.

Essential Responsibilities and Duties Include:

  • Create, develop and maintain the programming infrastructure (i.e., SOPs, standards, compliance).
  • Work with the Clinical Operations team to identify and implement processes that facilitate clinical project monitoring and reporting
  • Design, implement and maintain SAS code for data validation and edit checks
  • Implement and support statistical programming
  • Design, develop and maintain well-documented SAS code
  • Serve as a mentor for less experienced statistical programmers
  • Develop SAS procedures to automate data monitoring, data issue reporting, and data analysis
  • Produce periodic and ad hoc clinical data reports
  • Customize report templates to produce reports for data monitoring and quality control
  • Proactively look for ways to automate procedures to improve efficiency; drive continuous improvement and implement changes
  • Participate in the design of case report forms and recommend edit checks
  • Perform other TransMedics tasks and duties, as assigned


  • BS in Computer Science, Math, Statistics or equivalent quantitative discipline plus 12+ years of directly relevant experience; or equivalent combination of education and experience
  • Outstanding SAS expertise
  • Proven ability to write clear, robust code that is easy to maintain and modify
  • Proficiency in SAS MACRO functions
  • Strong SQL skills
  • Skilled in case report form design, databases programming, and data validation
  • Strong troubleshooting skills
  • Inquisitive and keen interest in data and data quality
  • Ability to multi-task, prioritize workload, handle changing priorities and to work calmly under time constraints and tight deadlines
  • Track record managing projects according to goals, schedule and budget
  • Self-motivated with strong work ethic
  • Demonstrated high level of attention to detail
  • Strong written and verbal communication skills.
  • Ability to work effectively with clinical managers, data managers and statisticians.
  • Excellent interpersonal skills
  • Medidata RAVE design experience a strong plus

BS in Computer Science, Math, Statistics or equivalent quantitative discipline

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