Senior Statistical Programmer II - R&I

WHY JOIN US?

At AstraZeneca we’re dedicated to being a Great Place to Work. Where you are empowered to push the boundaries of science and unleash your entrepreneurial spirit. There’s no better place to make a difference to medicine, patients, and society. An inclusive culture that champions diversity and collaboration, and always committed to lifelong learning, growth, and development. We’re on an exciting journey to pioneer the future of healthcare.

Recognizing the importance of individualized flexibility, our ways of working allow employees to balance personal and work commitments while ensuring we continue to create a strong culture of collaboration and teamwork by engaging face-to-face in our offices 3 days a week. Our head office is purposely designed with collaboration in mind, providing space where teams can come together to strategize, brainstorm and connect on key projects.

Our dedication to sustainability is also central to our culture and part of what makes AstraZeneca a great place to work. We know the health of people, the planet and our business are interconnected which is why we’re taking ambitious action to tackle some of the biggest challenges of our time, from climate change to access to healthcare and disease prevention.

Accountabilities:

As a Senior Statistical Programmer, you are responsible for leading programming deliverables of a clinical study or a small to medium sized clinical project. Typical accountabilities include:

• Quality, timely and efficient delivery of programming work for a study or project

• Implements statistical programming aspects of the protocol or clinical development program

• Ensures high quality is built into own deliverables and the quality delivered by other programmers

• Programs independently with high efficiency and quality

• Writes specifications and oversee completeness of relevant documentation

• Contributes to or drives the development of best practices to improve quality, efficiency and effectiveness within function

• Ensures compliance to standards and automation usage

• Plans and leads team activities and tasks

• Identifies, manages and communicates risk within the assigned studies and/or projects

• Works proactively with study team members including but not limited to the statistician, lead programmer, data manager and study leader

• Works cooperatively with contract programming providers

• Influences stakeholders by providing subject matter expertise on programming related items

• Contributes to or leads technical initiatives

• Employs project management practices in managing programming aspects of drug or technical projects

Education, Qualifications, Skills, and Experience:

• Degree in Mathematics (i.e., Applied Math, Engineering, etc), Statistics, Computer Science, Life Science, or equivalent

• Excellent programming skills in SAS (or R) and SAS macros

• Proficient knowledge of the clinical development process and industry standards (CDISC)

• Ability to apply programming knowledge to problem solving

• Ability to manage relevant documentation

• Ability to influence relevant stakeholders on Programming related items

• Current knowledge of technical and regulatory requirements relevant to the role

Desirable Skills/Experience:

• Broad experience across multiple therapeutic areas and across all phases of clinical trials

• Experience in regulatory submissions and interactions

SO, WHAT’S NEXT?

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 a great fit, please share this posting with them.
 

Great People want to Work with us! Find out why:

• GTAA Top Employer Award for 10 years

• Top 100 Employers Award

• Canada’s Most Admired Corporate Culture

• Learn more about working with us in Canada

• View our YouTube channel
   

Are you interested in working at AZ, apply today!

AstraZeneca is an equal opportunity employer that is committed to diversity and inclusion and providing a workplace that is free from discrimination. AstraZeneca is committed to accommodating persons with disabilities. Such accommodation is available on request in respect of all aspects of the recruitment, assessment and selection process and may be requested by emailing AZCHumanResources@astrazeneca.com.

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Date Posted

Closing Date

AstraZeneca embraces diversity and equality of opportunity.  We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills.  We believe that the more inclusive we are, the better our work will be.  We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics.  We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements.