Statistical Programmer

🚀 Hiring: Statistical Programmer – Clinical Data (SAS/R)

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Industry:

Experience:

About the Role

Statistical Programmer – Clinical Data

Key Responsibilities

• Lead statistical programming activities for assigned compounds or therapeutic areas
• Create and validate ADaM datasets, TFLs in compliance with CDISC standards
• Develop and validate ISS and ISE for regulatory submissions
• Build, test, and maintain reusable SAS programs and macros
• Prepare reviewer guides, define.xml, and regulatory documentation
• Mentor and guide junior statistical programmers
• Collaborate closely with Biostatistics, CDM, Clinical, and Regulatory teams

Required Skills & Experience

• Strong hands-on experience in

  SAS programming

  (R experience is a plus)
• In-depth knowledge of

  CDISC standards (ADaM, SDTM)

• Experience supporting

  FDA / EMA regulatory submissions

• Understanding of clinical trial processes and data flow
• Exposure to therapeutic areas such as

  Oncology, Immunology, or Neuroscience

• Strong communication and leadership capabilities

Why Join Us?

• Work on global, cutting-edge clinical trials
• Be part of a high-impact data-driven environment
• Collaborate with experienced professionals in life sciences

Interested candidates can share their CVs at:

samiksha@latinumhr.com