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.

Statistical Programmer 4+ Years(R)

R Biostatistical Programmer Role