Jobs at AstraZeneca

Supports strategic and tactical marketing for AstraZeneca’s GI Oncology franchise, including brand planning, promotional materials, digital engagement, competitive benchmarking, sales meetings, training, and medical conference coordination. The intern analyzes data, supports cross-functional projects, connects sales and marketing teams, and contributes to team engagement initiatives. This is a 12-month paid contract based in Mississauga with flexible onsite and virtual work.

Build and deploy AI-enabled business solutions for Oncology Business Excellence using Copilot, Power Platform, workflow automation, dashboards, and knowledge-management tools. Responsibilities include mapping workflows, prioritizing use cases, developing prototypes and AI agents, testing outputs, documenting requirements, supporting adoption, and measuring impact. The role collaborates with senior cross-functional stakeholders in a regulated biopharmaceutical environment.

Supports process engineering activities in a GMP radioconjugate manufacturing facility. Responsibilities include equipment checks, calibration coordination, automation troubleshooting, process improvement using Lean/Six Sigma, controlled-document authoring, production-data entry, small-scale trials, change controls, and technology-transfer activities. The intern will work onsite, follow radiation and aseptic safety requirements, and qualify as a Nuclear Energy Worker.

Supports regulatory submissions, Health Canada approval processes, product labeling, regulatory strategy, meeting preparation, and compliance activities for pharmaceutical products in Canada. Assists with Clinical Trial Applications, drug submissions, regulatory responses, policy monitoring, packaging artwork, and cross-functional initiatives, including digital and AI projects. Builds internal relationships, completes required training, and supports Regulatory Affairs efficiency and adherence to Good Regulatory Practice.

Supports digital and omnichannel marketing initiatives for AstraZeneca Canada, including digital asset coordination, Veeva PromoMats medical-legal-regulatory workflows, testing and publishing in Veeva CRM, website maintenance, quality assurance, stakeholder coordination, process documentation, and platform administration. The role provides exposure to pharmaceutical marketing operations, customer engagement, marketing technology, analytics, compliance, and responsible AI initiatives.

Supports global clinical study teams throughout study setup, conduct, maintenance, close-out, reporting, and archiving. Responsibilities include managing the electronic Trial Master File, regulatory submissions, study documents, tracking tools, clinical trial transparency activities, budgets, supplies, meetings, and inspection logistics. The intern also contributes to process improvement projects while ensuring compliance with ICH/GCP, company SOPs, and applicable regulations.

Leads regulatory submission planning, coordination, and execution across product lifecycles and global or regional markets. Provides regulatory guidance, reviews documentation, manages submission plans and tracking, identifies risks, coordinates cross-functional teams, supports compliance and document management, and contributes to process improvement. The role also provides coaching and knowledge sharing within the regulatory affairs team.

Lead site QA/QC and compliance for radiopharmaceutical manufacturing, ensuring cGMP adherence, inspection readiness, product release, CAPA management, quality metrics, continuous improvement, and development of quality staff and processes.

Leads the operational planning, execution, and reporting of pivotal, complex global clinical studies and Access to Medicine programs. Directs cross-functional study teams, manages timelines, budgets, risks, vendors, quality, compliance, governance, and inspection readiness. Provides operational strategy, senior stakeholder guidance, mentorship to study leads and managers, and oversight of clinical documents and data. Also contributes to process improvement initiatives within Development Operations.

Lead enterprise AI strategy and adoption across pharmaceutical R&D portfolio and project management. Identify use cases, guide pilots and scaled deployments, establish ROI and adoption metrics, and ensure privacy, security, ethics, and regulatory compliance. Partner with product, data, IT, legal, compliance, vendors, and global business teams while guiding data architecture, governance, change management, and responsible AI practices to improve portfolio decisions, capacity planning, cycle times, and patient impact.

Leads strategy, partner selection, due diligence, technology transfer, governance, supply continuity, and regulatory readiness for an external PET radiopharmaceutical manufacturing network. Oversees CDMOs, hospital radiopharmacies, academic sites, and commercial providers while coordinating with quality, regulatory, supply chain, procurement, legal, finance, and business development teams. Ensures compliant, reliable, scalable, and time-critical production and distribution across clinical and commercial programs.

Leads AstraZeneca Canada's national government relations strategy across federal, provincial, and municipal governments. The role shapes policy advocacy, advances medicine access and sector competitiveness, manages Innovative Medicines Canada engagement, advises executives, and communicates economic and societal impact. It also coordinates cross-functional stakeholders, builds external relationships, supports Ontario operations, and leads a geographically distributed government affairs team.

Leads daily vivarium operations supporting pharmaceutical research, including animal care, welfare, husbandry, facility readiness, radiation safety, containment, waste processing, and regulatory compliance. Oversees infrastructure, equipment, staff performance, training, and operational continuity. Provides scientific and technical leadership across drug development projects, collaborates with research, clinical, manufacturing, suppliers, and regulators, and may interpret pharmacokinetic, drug metabolism, ADME, and biomarker data.

Design, validate, and deploy publication-grade predictive and causal models for commercial and patient outcomes in rare disease. Build survival and time-series models, Bayesian marketing-mix and next-best-action systems, integrate Snowflake Cortex AI and AI agents, ensure HIPAA-compliant data operations, implement interpretability and bias guardrails, and translate insights to commercial stakeholders.

Lead end-to-end design research for complex digital health and clinical trial products. Guide cross-functional teams through research training and execution, conduct foundational, generative, and usability studies, translate technical workflows into user-centered artifacts, and ensure insights influence product roadmaps and design systems. Develop thought leadership through articles, white papers, and conference presentations, mentor junior researchers, explore AI-enabled research methods, and collaborate closely with product, design, and engineering teams.

Leads clinical supply chain planning for global Phase I–III programs, translating trial demand and enrollment forecasts into executable supply plans. Owns S&OP meetings, demand and supply reporting, manufacturing alignment, patient-dose planning, risk mitigation, budgeting support, and GxP-compliant SOPs. Partners across internal and external functions to improve planning workflows, systems, and change controls while ensuring supply visibility and proactively addressing shortages, bottlenecks, and timeline risks.

Design, deploy, and operate production-grade Generative AI agents and GenAI workflows for clinical trial optimization. Build scalable cloud infrastructure, automate via IaC and CI/CD, integrate LLM routing and monitoring (latency, token usage, hallucination detection), and collaborate with AI engineers and data scientists to move models from research to reliable production services.

Leads clinical regulatory writing across a portfolio, authors and reviews submission documents, develops submission communication strategies, and manages internal, external, and vendor writing teams. Interprets complex clinical data into clear regulatory messages, ensures technical and quality standards, collaborates across matrixed program teams, mentors colleagues, and drives continuous improvement and operational excellence within Clinical Regulatory Writing.