Territory Account Manager on the long - acting HIV Prevention Sales team at ViiV Healthcare. Driving results against business objectives and partnerships with HCPs and cross - functional teams.
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196 jobs found
Supplier Quality Audit Lead managing GMP and Quality Systems compliance audits for GSK manufacturing suppliers. Responsible for maintaining supplier compliance and effective communication with stakeholders.
Lead government affairs and market access strategies for ViiV Healthcare in Canada. Build trusted relationships and ensure patient access to innovative therapies through effective policy solutions.
Quality Inspection Readiness Director ensuring regulatory compliance and continuous improvement at GSK. Collaborating with teams to maintain inspection readiness across global sites.
Director of Translational Science at GSK focusing on Respiratory, Immunology, and Inflammation. Leading biomarker strategies and cross - functional collaborations for drug development.
Lead medical writing for oncology assets at GSK while ensuring high - quality regulatory documents and compliance. Collaborate with cross - functional teams, driving timely submissions and innovations.
Leading global analytical standards for medicines network at GSK in Belgium. Collaborating with cross - functional teams to improve patient safety and analytical practices.
VP, Chief Enterprise Architect responsible for enterprise - wide architecture and digital transformation at GSK. Driving AI scale and influencing business strategy across global operations.
Director responsible for managing global content design and delivery for Oncology. Leading integrated medical communication plans and collaborating with cross - functional teams.
Finance Analyst joining GSK's Group FP&A team to support financial planning and forecasting processes. Collaborating with finance partners to deliver actionable insights and process improvements.
Director of State Government Affairs influencing changes to state laws for GSK's pharmaceutical priorities. Engaging with key stakeholders to align state laws with public health initiatives.
Medical expert evaluating safety and managing risk for projects in clinical development and post - marketing. Collaborating with scientists and clinical teams to support safety assessments and regulatory documentation.