Job Description
As a Senior or Principal Statistical Programmer in our sponsor-dedicated Flexible Solutions business unit, you will be central to the successful delivery of complex global oncology clinical trials (Phases I–III) for some of the world's most renowned and innovative pharmaceutical companies.
In this role, you will contribute to the development of new and life-changing oncology therapies by developing and validating SAS programs for data analysis and reporting, supporting submissions, regulatory responses, publications, and post-hoc requests.
Your expertise will directly impact the advancement of oncology treatments and the lives of thousands of patients around the world.
You can be 100% home-based, or if you prefer, work from one of our local offices in your home country.
Your Responsibilities
Perform programming activities for oncology clinical trials, ensuring quality, accuracy, and compliance with study timelines and regulatory standards.
Review SAPs and TFL shells f...
In this role, you will contribute to the development of new and life-changing oncology therapies by developing and validating SAS programs for data analysis and reporting, supporting submissions, regulatory responses, publications, and post-hoc requests.
Your expertise will directly impact the advancement of oncology treatments and the lives of thousands of patients around the world.
You can be 100% home-based, or if you prefer, work from one of our local offices in your home country.
Your Responsibilities
Perform programming activities for oncology clinical trials, ensuring quality, accuracy, and compliance with study timelines and regulatory standards.
Review SAPs and TFL shells f...
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