Job Description

Senior Clinical Programmer IHybrid Work- on average 3 days/week from officeMinimum 1 day from our Mississauga office and 2 days from our Mississauga or Downtown (temporary) officeAt AstraZeneca, we pride ourselves on crafting a collaborative culture that champions knowledge-sharing, ambitious thinking and innovation ultimately providing employees with the opportunity to work across teams, functions and even the globe.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 were taking ambitious action to tackle some of the biggest challenges of our time, from climate change to access to healthcare and disease prevention.Introduction to roleAs a Senior Clinical Programmer I, you will be at the forefront of programming, dashboard development, and validation of data cleaning and review listings for ongoing clinical studies. This role demands high technical skills and industry knowledge to independently perform programming tasks while exercising judgment in complex situations. You will also contribute to cross-functional initiatives with high complexity, ensuring the seamless integration of data and technology in clinical trials.AccountabilitiesResponsibilities include (but are not limited to) the design, development, implementation, and validation of complex programs created in SAS/Python/R or dashboard applications such as PowerBI/Spotfire.Program independently with efficiency and quality to process, analyze, and report clinical trial data ready for review by clinical study teamsSupply to the design, development, and implementation of highly complex projects or initiatives that are included in the clinical programming roadmapDefine and build vital processes and tools to perform clinical programming activities for both global and study-level analytical solutionsDevelop standard processes that enhance quality, efficiency, timelines, and effectiveness within the functionProvide technical expertise, cross-training, and support as required to ensure the availability and performance of developed reports and dashboards for both external and internal usersSupervise the documentation of programming tasks, ensuring compliance with standard operating procedures and established guidelines.Ensure high quality is built into work and quality delivered by other programmersIdentify and communicate risk within assigned studies and/or projectsCollaborate with various teams including data management, development operations, clinical, biometrics, and other relevant cross-functional teams supporting clinical trials to deliver end-user reporting needsDevelop and maintain data visualization tools including requirements gathering, data provisioning, and building dashboards as neededCreate and maintain a catalog of reports to aid data cleaning and reporting activitiesEssential Skills/ExperienceBachelors/Masters degree or equivalent in a STEM field (science, technology, engineering and mathematics)Accomplished programming skills in at least 2 of the following languages: SAS, Python, R, SQLSkilled in Power BI/SpotFire or other dashboard technologiesIntermediate knowledge of clinical development process and industry standardsAt least 6 years of relevant experienceAbility to influence relevant stakeholdersExcellent analytical and critical thinking skills, writing, communication skills, and ability to work within a cross-functional, global teamTechnical expertise with data capture, data models, data mining, and visualization techniquesPrior experience and understanding of EDC systems like Medidata Rave / Inform / Veeva and Data Platforms like Saama/Entimice, SAS LSAF etc.Desirable Skills/ExperienceExcellent collaborative skills and the ability to manage complexity and change in a dynamic environmentBroad knowledge of FDA regulations and GCP/ICH guidelines as related to clinical programming processesExperience in producing analytical dashboards with Power BI, Spotfire or other Business Intelligence toolsKnowledge on MicroStrategyGreat People want to Work with us! Find out why: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 .#LI-HybridDate Posted 11-Feb-2025Closing Date 27-Feb-2025AstraZeneca 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.

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