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Clinical Programming Specialist

1 week ago

Bengaluru, Karnataka, India Trigent software ltd Full time

Role Overview:

The Senior/Principal Stat Programmer will be responsible for leading the development of clinical trial data management plans, creating case report forms, annotating CRFs, developing SDTM and ADaM datasets using SAS, and generating tables, listings, and graphs to support clinical study reports, posters, and manuscripts. The ideal candidate will have strong analytical skills, excellent communication abilities, and the ability to work independently with minimal supervision.

Main Responsibilities:

  • Design and implement data management strategies for clinical trials.
  • Develop and maintain SDTM and ADaM datasets using SAS.
  • Create electronic submission packages for regulatory agencies.
  • Collaborate with statisticians to interpret data and provide insights.
  • Lead the programming team and contribute to department initiatives.
  • Train and mentor junior team members.

Requirements:

  • Bachelor's or Master's degree in Statistics, Mathematics, Computer Science, Electrical Engineering, Biotechnology, or related field.
  • Minimum 8-13 years of experience in Statistical Programming in Clinical domain.