GSK is a global healthcare company focused on advancing science and technology to develop innovative medicines, vaccines, and consumer health products to improve patient outcomes.
London, England
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Hybrid · Mississauga
Manage the execution of clinical trials from start-up through close-out in accordance with Good Clinical Practice, study budgets, and timelines. Collaborate with study teams to monitor progress, resolve risks, and ensure inspection readiness of clinical documentation.
Hybrid · Québec
The Expert Standards LMSAT acts as a technical reference for implementing and maintaining LMSAT standards, including process validation, cleaning validation, and contamination control. They provide coaching to site teams, contribute to global standard development, and monitor performance indicators to ensure operational excellence.
Hybrid · Mississauga
Provide scientific leadership for study design, protocol development, data review, interpretation, and clinical and regulatory documentation within the asset strategy set by the Clinical Development Lead. Collaborate with cross-functional teams and external stakeholders to support study execution, scientific quality, data integrity, and programme-level insights.
Hybrid · Mississauga
The Clinical Operations Asset Lead serves as the single point of accountability for clinical operations delivery across the full asset lifecycle. They drive operational strategy, lead study delivery teams, and ensure high-quality, on-time execution of clinical programs.
Hybrid · Québec
The project manager for technical services acts as an expert for production equipment, overseeing installation, performance, and reliability. They lead root cause investigations, develop technical solutions, and ensure compliance with quality and safety standards.
Hybrid · Mississauga
The Commercial Oncology Pipeline Director leads the Canadian commercial strategy for a multi-brand oncology portfolio across all lifecycle stages. They serve as the primary interface between Canadian stakeholders and global teams to ensure launch readiness and maximize asset value.
On-site · Québec
The intern will contribute to the development and integration of technical solutions within building processes while ensuring compliance with site standards. Responsibilities include drafting technical documents, coordinating project activities, and participating in quality investigations and risk analyses.
Hybrid · Mississauga
The role involves building trusted scientific relationships with clinicians and communicating evidence-based information to support clinical decision-making. Additionally, the incumbent will gather clinical insights and identify potential investigators to support clinical development activities.
Remote · Alberta, Canada, British Columbia, Canada, Manitoba, Canada, Ontario, Canada, Saskatchewan, Canada
Lead and inspire a high-performing regional team of Key Account Managers to achieve sales targets and execute business strategies. Build strong partnerships with external stakeholders and collaborate with cross-functional teams to deliver science-based solutions.
Hybrid · Mississauga
The Associate Director will lead the operational strategy and delivery for complex oncology late-phase clinical assets. They will coordinate cross-functional inputs and maintain inspection readiness while ensuring high-quality, regulatory-grade data.
Hybrid · Hamilton
The Marketing Associate Intern will support the planning and execution of strategic and operational priorities for the Severe Asthma and Nasal Polyps portfolio. Responsibilities include managing omnichannel marketing tactics, tracking budgets, analyzing performance data, and coordinating cross-functional project workflows.
Hybrid · Mississauga
The Global Study Manager is accountable for the end-to-end operational delivery of clinical studies, ensuring they meet time, quality, and budget requirements. They lead matrix teams and oversee vendor performance while maintaining compliance with regulatory standards and GSK SOPs.
Hybrid · Mississauga
The Medical Director serves as the physician within the clinical programme team, providing medical expertise for study design, safety oversight, and data interpretation. They lead medical monitoring activities and collaborate with cross-functional teams to ensure clinical integrity and regulatory compliance.
Hybrid · Québec
The Technology and Process Lead is responsible for the strategic and operational direction of a technical team supporting vaccine and adjuvant manufacturing. They ensure technical governance of processes and equipment while collaborating with cross-functional teams to maintain compliance and operational excellence.
Hybrid · Québec
The Master Supply Chain Planner is responsible for developing and optimizing strategic and tactical production and supply plans for the Ste-Foy site. They act as the primary point of contact between the site and global supply chain teams to ensure product availability and operational continuity.
Hybrid · Mississauga
The Regulatory Affairs Manager is responsible for developing regulatory strategies and managing a portfolio of products to ensure timely approvals and compliance with Health Canada guidelines. They will lead submission activities, influence global and local functions, and mentor junior staff to achieve commercial and regulatory objectives.
Hybrid · Mississauga
The Medical Director serves as the physician within the clinical program team, providing medical expertise for study design, conduct, and safety oversight. They lead medical monitoring activities and collaborate with cross-functional teams to ensure clinical integrity and regulatory compliance.
Hybrid · Québec
You will gain hands-on experience in pharmaceutical production, engineering, quality, and supply chain management while contributing to global manufacturing operations. You will also lead initiatives to improve efficiency, safety, and sustainability using advanced technologies and data-driven methodologies.
Hybrid · Québec
You will work on cross-functional projects and rotations involving manufacturing equipment, utility services, and digital systems to drive automation and efficiency. Your role includes managing automation projects, implementing smart manufacturing solutions, and ensuring compliance within a highly regulated pharmaceutical environment.
Hybrid · Mississauga
You will lead the operational delivery of global clinical studies in Canada by coordinating cross-functional teams and managing study timelines, budgets, and site activation. Additionally, you will act as the primary point of contact for sites, ensuring compliance with regulatory standards and driving recruitment targets.
