Job Description

Responsibilities and Requirements:

Develop and maintain SAS programs to import, clean, and validate clinical trial data.

Use R for data manipulation, analysis, and visualization.

Perform statistical analyses in accordance with study protocols and analysis plans.

Generate tables, listings, and figures (TLFs) using SAS and R.

Create and QC statistical outputs and clinical study reports for regulatory submissions.

Document programming activities and ensure compliance with Standard Operating Procedures (SOPs).

Work closely with biostatisticians, data managers, and clinical researchers.

Provide programming support for ad-hoc analysis requests and exploratory data analyses.

Perform rigorous quality checks on all deliverables.

Minimum of 5years of experience working for large pharma's/CROs .

Job Tags

Permanent employment,

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