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Senior Statistical Programmer

New

Skills

21CRF Part 11 ADaM standards Clinical database structures E-Submission Standards ICH guidelines ISO 9001:2000 SAS Base SAS Macros SAS programming SDTM standards

Join MMS, an award-winning clinical research organization, as a Senior Statistical Programmer. This remote role offers the opportunity to work with a collaborative team focused on delivering high-quality data solutions for the pharmaceutical and biotech industries. You will leverage your expertise in SAS programming to generate tables, listings, and graphs from clinical trial databases while adhering to industry standards.

Key Responsibilities
  • Generate tables, listings, and graphs from clinical trial databases using SAS.
  • Utilize System Development Life Cycle (SDLC) for programming deliverables.
  • Lead study or small programming project teams and manage tasks to achieve objectives.
  • Provide guidance to junior colleagues and contribute to continuous improvement efforts.
Required Skills & Qualifications
  • Mastery in SAS programming, SAS Base, and SAS Macros.
  • Advanced knowledge of E-Submission Standards, SDTM, and ADaM standards.
  • 5-9 years of experience in clinical programming within the pharma or CRO industry.
  • Strong organizational and communication skills.

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Job Type: Remote

Salary: Not Disclosed

Experience: Entry

Duration: Months

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