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Clinical Data Scientist I

Salary undisclosed

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Overview

The Clinical Data Scientist I is responsible for analyzing clinical trials or healthcare data, identifying trends and patterns, and developing predictive models to support clinical decision-making. The Clinical Data Scientist I will work closely with cross-functional teams, including clinical research associates, biostatisticians, and software engineers, to ensure the accuracy and completeness of clinical trial data and to identify opportunities for leveraging data to drive clinical insights.

Responsibilities

· Collecting and cleaning clinical trial data from various sources.

· Conducting analyses and programming under the guidance of a senior data scientist.

· Assisting with the preparation of clinical/RWE study reports, manuscripts, and other scientific documents.

· Participate in development of R codes and packages for clinical trials.

· Perform validation of codes and analysis.

· Independently develop and debug simple to complex R programs in a timely manner.

· Independently implement statistical analysis, data preparation, and data manipulation into R programs and packages.

· Independently create statistical tables, figures, and listings in R for clinical trial data.

· Create and maintain documentation for R programs and validation results.

· Performs additional tasks as assigned.

Job Requirements

Education

· A Master or Ph.D. degree in statistics, biostatistics, math/computer sciences, or a related field.

Experience

· 1+ years of experience in data sciences or research or drug industry using statistical analysis software.

· Experiences in R-shiny, SAS, Python, clinical trials are plus.

Skills and Competencies

· Basic knowledge of clinical research/RWE and regulatory requirements.

· Strong written and verbal communication skills.

· Ability to work independently and as part of a team.

· Strong organizational skills and attention to detail.

· Willingness to learn and adapt to new technologies and processes.

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