R Biostatistical Programmer Role

Description

We are seeking a skilled R Biostatistical Programmer to join our dynamic team in India. The ideal candidate will have 2-8 years of experience in statistical programming, specifically in the pharmaceutical or biotechnology sectors, and will play a crucial role in supporting clinical trials and research studies through rigorous data analysis and statistical reporting.

Responsibilities

• Develop and maintain statistical programming code in R for clinical trials and research studies.
• Generate and validate statistical outputs including tables, listings, and figures for clinical study reports.
• Collaborate with biostatisticians and data managers to ensure accurate and timely delivery of data analyses.
• Participate in the preparation of statistical analysis plans and contribute to protocol development.
• Ensure compliance with regulatory requirements and internal standard operating procedures (SOPs).
• Perform quality control checks on statistical outputs and programming code.
• Document programming processes and maintain effective communication with team members.

Skills and Qualifications

• 2-8 years of experience in statistical programming, preferably in the pharmaceutical or biotechnology industry.
• Proficiency in R programming language and its statistical packages.
• Strong understanding of clinical trial methodologies and biostatistical concepts.
• Experience with data manipulation and analysis in R, including data wrangling with packages such as dplyr and tidyr.
• Knowledge of SAS or other programming languages is a plus.
• Familiarity with regulatory guidelines (e.g., ICH, FDA) related to statistical programming and clinical trials.
• Excellent problem-solving skills and attention to detail.
• Effective communication skills, both written and verbal, to convey complex statistical information clearly.