Future Tech Jobs
Future Tech Jobs
Interventional Study Scientist Medical DirectorLocations– GSK HQ UK, New Oxford Street & USA - Upper Providence/ Waltham MAReports to: Head of Interventional & Supported StudiesJoin GSK's Medical Affairs team and be part of a global organization that drives innovation, scientific...
Interventional Study Scientist Medical DirectorLocations– GSK HQ UK, New Oxford Street & USA - Upper Providence/ Waltham MAReports to: Head of Interventional & Supported StudiesJoin GSK's Medical Affairs team and be part of a global organization that drives innovation, scientific...
The SERM Scientific Director role involves leading pharmacovigilance and risk management strategies for clinical development and post-marketing products. Responsibilities include evaluating safety data, managing safety concerns, and supporting regulatory activities. The role operates in a global, cross-functional environment and may include mentoring responsibilities.
The role involves leading the development and strategy of AI-enabled digital products for structured authoring and regulatory content across clinical, non-clinical, CMC, safety, and publications domains. The Product Director will drive innovation in automated content generation, modular reuse, and compliance within a GxP environment, working closely with cross-functional stakeholders and technical teams to scale enterprise-grade solutions.
This role leads the global development of a respiratory medicine from clinical proof of concept through to approval, serving as the strategic and operational leader of a cross-functional matrix team. The VP Medicine Development Leader defines the asset’s vision, drives evidence-based decision-making, and ensures alignment across R&D, manufacturing, regulatory, and commercial functions to deliver differentiated medicines for patients. The position involves shaping development plans, managing budgets, engaging with regulators, and supporting lifecycle strategies while representing the asset to senior leadership and external stakeholders.
The Regional Regulatory Manager leads the development and execution of regional regulatory strategies for assigned assets, ensuring alignment with global goals and regional requirements. This role involves close collaboration with global and local teams, providing regulatory expertise, anticipating risks, and driving timely submissions and approvals.
The Regional Regulatory Manager leads the development and execution of regional regulatory strategies for assigned assets, ensuring alignment with global strategies and regional requirements. This role involves close collaboration with global and local teams to deliver timely, compliant regulatory submissions and approvals, while providing regulatory expertise and market insights to support decision-making and risk management.
The Regional Regulatory Manager leads the development and execution of regional regulatory strategies for assigned assets, ensuring alignment with global strategies and regional requirements. This role involves close collaboration with global and local teams, providing regulatory expertise, managing submissions and approvals, and driving cross-functional alignment to deliver best-in-class regulatory outcomes.
The Regional Regulatory Manager leads the development and execution of regional regulatory strategies for assigned assets, ensuring alignment with global strategies and regional requirements. This role involves close collaboration with global and local teams, providing regulatory expertise, managing submissions and approvals, and driving continuous improvement and innovation.
This role leads the global development of a respiratory medicine from clinical proof of concept through to regulatory approval, serving as the primary accountable leader across a matrixed cross-functional team. The VP will define strategic direction, oversee clinical and regulatory planning, manage budgets, and ensure alignment with GSK’s broader R&D and commercial objectives. The position involves high-level stakeholder engagement, lifecycle planning, and external representation to regulators and advisory bodies.
Lead the global development of a respiratory medicine from clinical proof of concept through to first-market approval, serving as the single point of accountability. You will build and lead a cross-functional matrix team, define strategic direction, and ensure alignment with GSK’s R&D and commercial strategies. The role involves shaping lifecycle plans, making evidence-based go/no-go decisions, and engaging with regulators and senior leadership to deliver patient-focused medical solutions.
Leads global development of a respiratory medicine from clinical proof of concept to approval, aligning cross-functional teams across R&D, manufacturing, and commercial functions. Defines strategic vision, manages development plans, regulatory submissions, and lifecycle strategy while ensuring patient-focused innovation and compliance. Acts as primary point of accountability and spokesperson to senior leadership and external stakeholders.
This role leads the global development of a respiratory medicine from proof of concept through to approval, serving as the primary accountable leader across a cross-functional matrix team. The VP will define strategic direction, oversee clinical and regulatory execution, and align development with GSK’s broader R&D and commercial strategy, while engaging with senior leadership and external stakeholders to advance patient-focused innovation.
Leads global development of a respiratory medicine from clinical proof of concept through approval, serving as the primary accountable leader across a cross-functional matrix team. Defines strategic vision, drives evidence generation, lifecycle planning, and regulatory strategy while coordinating input from R&D, manufacturing, commercial, and regulatory stakeholders to deliver patient-focused therapies.
The SERM Scientific Director will lead the safety evaluation and risk management of GSK's key assets, ensuring scientifically sound review and interpretation of data. They will develop and execute safety strategies, manage safety governance, and represent GSK on cross-functional teams to address product safety issues and improve regulatory adherence.
