Master SAS Programmer
4 days ago
We are seeking a highly skilled Senior SAS Programmer with extensive lead and co-lead experience in oncology clinical trials. The ideal candidate will be able to work independently, write specifications, and contribute to the overall success of our clients' clinical trials.
Key Responsibilities:
- Lead and Co-Lead Studies: Collaborate closely with statisticians to ensure timely and accurate delivery of outputs.
- SAS Programming: Develop, test, and validate SAS programs to support clinical trials, ensuring high-quality data management and statistical analysis.
- Oncology Expertise: Apply your in-depth knowledge of oncology clinical trials to provide insights and support for study designs and analyses.
- Data Management and Analysis: Create and manage datasets, generate tables, listings, and figures, and ensure the integrity and accuracy of clinical trial data.
- Spec Writing: Write detailed specifications for datasets, outputs, and analysis, ensuring compliance with regulatory standards and guidelines.
Benefits Include:
- A competitive salary range of $120,000 - $160,000 per annum, depending on experience.
- Opportunity to work on complex projects and develop your skills in oncology-focused clinical trials.
- Collaborative and dynamic work environment.
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