Sr Statistical Programmer

4 weeks ago

Bengaluru, India Trigent Software - Professional Services Full time
Location: Remote

Experience: 5+ Years in Statistical Programming

Immediate Joiner

Responsibilities:

- Develop & Validate Programs: Create and validate statistical programs using SAS and/or R for clinical trial data analysis.- Experience in clinical trial datasets both creation and validation (e.g., SDTM, ADaM) and CDISC standards.- Data Analysis & Reporting: Provide programming support for clinical study reports, tables, listings, and figures.- Collaborate with Teams: Work closely with biostatisticians to ensure accurate data analysis and timely reporting.- Regulatory Compliance: Ensure adherence to FDA, EMA, and other regulatory guidelines.- Documentation: Assist in the creation and maintenance of specifications, SOPs, and project documentation.

Requirements:

- 5+ Years of Experience in statistical programming, preferably within clinical trials.- Proficiency in SAS and/or R; experience with other programming languages is a plus.- Strong understanding of- Experience in a CRO or pharmaceutical company is preferred.

Excellent Communication Skills and ability to collaborate in a global team.

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