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What you will be doing
- Collaborating with statisticians and programmers to develop and validate statistical programs for clinical trial data analysis.
- Assisting in the creation of statistical analysis plans and specifications.
- Programming, testing, and documenting statistical programs in accordance with regulatory guidelines.
- Conducting quality control checks on statistical outputs to ensure accuracy and reliability.
- Supporting the preparation of data sets and statistical reports for regulatory submissions.
Your profile
- Bachelor’s degree in Statistics, Computer Science, or related field.
- Proficiency in programming languages such as SAS, R, or Python.
- Strong analytical and problem-solving skills.
- Knowledge of clinical trial data structures and statistical methodologies.
- Excellent communication and teamwork abilities.
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