Oncology Statistical Programming – Senior Programmer and Associate Director Opportunities at AstraZeneca

Do you have a strong expertise and passion for Programming? Are you looking to make a significant impact on all phases of drug development and regulatory interactions? Join AstraZeneca, where science and innovative ideas turn into life-changing medicines!

About AstraZeneca

AstraZeneca is a global, science-led, patient-centric biopharmaceutical company focused on the discovery, development, and commercialization of prescription medicines. Join our dedicated Oncology team with the ambition to eliminate cancer as a cause of death. Our innovative pipeline spans multiple indications and high-quality molecules at all stages, continually advancing to conquer cancer through data-driven, evidence-based decisions.

What You’ll Do

As part of the Oncology Biometrics Programming department, you will provide statistical programming support and leadership in analysis and reporting of clinical trials. Your work will involve clinical study report development, regulatory submissions, commercialization, and scientific utilization of data for AstraZeneca products.

We offer career opportunities at both the Senior Programmer (SP) and Associate Director (AD) levels.

Responsibilities

• Lead (AD) or contribute (SP) to the delivery of Clinical Study Reports (CSR), Study Data Tabulation Model (SDTM)/Analysis Data Model (ADaM) databases, and Tables, Figures, and Listings (TFL) outputs, in compliance with data standards and regulations.
• Lead (AD) or contribute (SP) to statistical programming deliverables for regulatory submissions, including pooled safety/efficacy databases, outputs, responses to regulatory questions, commercialization, and reimbursements.
• Lead (AD) or contribute (SP) to the development of standard processes to enhance quality, efficiency, and effectiveness within the Oncology Programming group.
• Lead (AD) or contribute (SP) to Development Safety Update Reports (DSUR), Periodic Benefit-Risk Evaluation Reports (PBRER), and Investigator’s Brochures (IB).

Essential for the Role

To succeed, you should be an enthusiastic individual with a good grasp of the technical and regulatory requirements in programming within the pharmaceutical or healthcare industry. You should enjoy multitasking, collaborating as part of a distributed team, and solving problems effectively.

Desirable Experience Includes:

• BSc in a Mathematical, Statistical, Computer Science, or Life Science subject.
• Excellent problem-solving skills.
• Attention to detail and ability to manage concurrent projects and activities diligently.
• Exceptional verbal and written communication skills with the ability to influence stakeholders.
• Extensive SAS programming expertise gained in a clinical drug development or healthcare setting.
• Comprehensive knowledge of technical and regulatory requirements with submission experience.
• Knowledge of CDISC standards and industry practices.
• A team-centric approach with an appreciation for the roles, skills, and strengths of team members.
• Experience working on Oncology clinical trials and related data.

Why AstraZeneca?

At AstraZeneca, we’re dedicated to creating a Great Place to Work. Here, you are empowered to push the boundaries of science and unleash your entrepreneurial spirit. Our inclusive culture champions diversity, collaboration, and lifelong learning, committed to pioneering the future of healthcare.

So, What’s Next?

If you’re already envisioning yourself as part of our team, we’re excited to hear from you!

Competitive Salary and Benefits Package

The successful candidate will have access to a flexible employee benefits fund, including holiday purchase, flexible time off, pension contributions, Share Save plans, a performance recognition scheme, and a competitive, generous remuneration package.

Where Can I Find Out More?

Stay connected with us on Social Media:

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Visit our Biometrics dedicated webpage: