Senior Statistical Programmer - Oncology
Location: Cambridge or Macclesfield, UK
Competitive salary and benefits
Senior Statistical Programmer, Oncology
Do you have passion for Programming? Do you consider yourself an SME? Would you like to apply your skills to impact drug development process and regulatory interactions in a company that follows the science and turns ideas into life-enhancing medicines? Then AstraZeneca might be the one for you!
AstraZeneca is a global, science-led, patient-centric biopharmaceutical company passionate about the discovery, development, and commercialization of prescription medicines. Join the team dedicated to Oncology, with an ambition to eliminate cancer as a cause of death. With multiple indications and high-quality molecules in all stages of our innovative pipeline, we keep pushing forward to conquer cancer through data, innovation and evidence-based decisions.
Role
You will be working in the Oncology Biometrics Programming department providing statistical programming support and/or leading activities related to the analysis and reporting process at project/study level for the delivery of the statistical programming aspects of clinical development. The scope of work includes, but is not limited to, clinical study report development, regulatory submissions, commercialization, and the scientific utilization of our data for AstraZeneca products. There are many career options that you can pursue for your development and progression.
Crucial for the role
To succeed in this role, you need to be a hardworking individual with an understanding of technical and regulatory requirements related to programming within the pharmaceutical or healthcare industry. You should have the ability to multitask, collaborate as part of a team that operates globally and have an appetite for solving problems.
- Bachelor's or Master's (or local equivalent) degree in Mathematics, Statistics, Computer Science, Life or Social Sciences or related field
- Ability to pay attention to detail and lead/work on concurrent studies and activities
- Excellent verbal and written communication skills and ability to influence team members
- Extensive SAS programming expertise to a high level within clinical drug development
- Ability to work independently on the assigned programming tasks
- Extensive knowledge of technical and regulatory requirements
- Good knowledge of CDISC standards and industry processes
- Experience leading studies or activities in clinical trials
Next Steps - Apply today!
To be considered for this exciting opportunity, please complete the full application on our website at your earliest convenience - it is the only way that our Recruiter and Hiring Manager can know that you feel well qualified for this opportunity. If you know someone who would be an excellent fit, please share this posting with them.
Where can I find out more?
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