Parexel
Senior Statistical Programmer
Overview
The Senior Statistical Programmer provides technical expertise for the conduct of clinical trials, acts as an internal subject matter expert in specific areas providing technical support and expert advice, and works independently to support various programing activities related to the analysis and reporting of clinical study data.
About Parexel
Parexel is a leading global clinical research organization (CRO) providing insights-driven Clinical and Consulting solutions to the world’s life sciences industry. Leveraging deep local knowledge and a global breadth of clinical, regulatory and therapeutic expertise, our professionals worldwide work in partnership with biopharmaceutical leaders, em
Requirements & Eligibility
- University degree
- Strong written and verbal English communication skills
- Proficiency in SAS
- Excellent analytical skills
- Ability to successfully lead a global team
- Extensive knowledge and understanding of the programming and reporting process
- Knowledge of SOPs/Guidelines, ICH-GCP, and any other applicable local and international regulations such as 21 CFR Part 11
Key Responsibilities
- Ability to fill Statistical Programming Lead role on projects
- Input into and negotiate statistical programming timelines and ensure that timelines are adhered to
- Coordinate and lead a statistical programming team to successful completion of a study within given timelines and budget
- Monitor project resourcing, project budgets, and identify changes in scope
- Use efficient programming techniques to produce/QC derived datasets (e.g. SDTM, ADaM), tables, figures, and data listings
- Ensure quality control (QC) is performed on all process and technical activities
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