12-month contract
At 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 and BlueSky Hub in downtown Toronto are 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.
Introduction to the role: The Biopharma Study Management Operations Intern is a member of extended global study team supporting delivery of clinical studies within Global Medicines Development (GMD) to time, cost, and quality, from Clinical Study Protocol (CSP) development through study set-up, maintenance, close-out, development of Clinical Study Report (CSR) to study archiving. The intern supports Global Study Associate Director (GSAD) and Global Study Managers (GSM) in delegated aspects of clinical study execution in accordance with the Study Team Operating Model (STOM), AZ Project Management Framework, current clinical trial regulations (e.g., ICH GCP), AstraZeneca Standard Operating Procedures (AZ SOPs), AZ policies and standards (e.g.



AZ guidelines) and in line with AZ values and behaviours.
This role is a 12-month paid contract position, which starts in January 2027 and will end in December 2027.
This position will be based in our Mississauga head office and allow for adaptable working arrangements working both onsite (3 times per week) and virtually.
Key Responsibilities may include: Support Global Study Associate Directors and Global Study Managers by completing delegated study work.
Initiate and be responsible for the set-up of the electronic Trial Master File (eTMF). Maintain and close the eTMF to ensure compliance to International Conference of Harmonization Guidelines for Good Clinical Practice (ICH/GCP) and AZ SOPs
Interact/collaborate with Site Management & Monitoring, other internal staff and external vendors in collection of regulatory and other essential documents.
Contribute to electronic applications/submissions in ANGEL by crafting and handling clinical regulatory documents according to the requested technical standards and supporting effective publishing and delivery to regulatory authorities. Proactively plan and collate the administrative appendices for the CSR
Initiate and maintain production of study documents, ensuring template and version compliance per study specific requirements
Set-up, populate and accurately maintain information in AstraZeneca tracking and communication tools (e.g. IMPACT, SharePoint, BOX if used,



MS teams and study team shared mailbox) and support team members in the usage of these tools
Support the set-up, maintenance and close-out of Clinical Trial Transparency (CTT) activity in PharmaCM, coordinating with relevant partners to fulfil AstraZeneca compliance and meet the regulatory authority needs
Support the Global Study Leader with tracking, reconciliation and follow-up of the study's budget/payments in relevant systems (e.g. Coupa, FIND)
Contribute to application, coordination, supply and tracking of study materials and equipment. Internal BioPharmaceuticals Clinical Operations Job Description
Contribute to collection of study supplies if required at the study close-out
Coordinate administrative tasks and logistic support throughout the conduct of the study, audits and regulatory inspections, according to company policies and SOPs
Lead practical arrangements, coordination and assist in preparing meetings both within the organization and with outside parties. Examples include study team, committee, monitor, Investigator, and virtual meetings. Liaise with internal and external participants and/or vendors
Prepare and contribute and distribute presentation material for meetings, newsletters and web sites
Work on non-drug project work in process improvements and/or leading improvement projects as discussed and agreed upon with their manager.
Qualifications: Education in medical or biological sciences or specialty associated with clinical research preferred;
Confirmed organizational and analytical skills
Previous administrative training/experience
Computer proficiency in day-to-day tasks
Develop working knowledge of the Clinical Study Process and an understanding of the…

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📌 Biopharma Study Management Operations GSA Intern (Ontario)
🏢 AstraZeneca
📍 Ontario