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Senior SAS Programmer - Clinical Trials Lead
Job summary
A global biopharmaceutical services company is seeking a Senior Statistical Programmer in the UK. This role involves creating SAS programs, providing programming support for clinical trials, and ensuring the quality of deliverables while adhering to regulatory standards. The ideal candidate has a Bachelor's degree in a related field and at least 5 years of experience in clinical programming. Join us to make a significant impact in clinical development.
Qualifications
- Minimum of 5 years clinical/statistical programming experience in pharmaceutical clinical development.
- In-depth understanding of clinical data structure (e.g., CDISC standards).
- Demonstrated ability in handling and processing upstream data.
Responsibilities
- Create SAS programs for analysis datasets and outputs.
- Provide programming support for project teams.
- Review key planning documents for programming requirements.
Skills
Education
Tools
* The salary benchmark is based on the target salaries of market leaders in their relevant sectors. It is intended to serve as a guide to help Premium Members assess open positions and to help in salary negotiations. The salary benchmark is not provided directly by the company, which could be significantly higher or lower.