Latest Drug Discovery Jobs

Senior Director, Portfolio Integration Lead

Leads scientific and strategic integration across multiple oncology development programmes, ensuring alignment with disease biology, biomarker strategies, and clinical innovation. Acts as a cross-asset expert, shaping portfolio-level decision-making and advancing trial design through emerging technologies like AI. Works closely with Clinical Development Leads and senior governance to drive coherent, efficient development across GSK’s oncology pipeline.

GSK

Hybrid Permanent

Senior Director, Portfolio Integration Lead

This role involves providing scientific leadership across GSK’s oncology portfolio, ensuring strategic alignment and integration of multiple clinical development programmes. The Senior Director will drive innovation in trial design, biomarker strategies, and data-driven decision-making while collaborating with cross-functional teams and external experts. The position focuses on advancing cancer treatments with high unmet need through a pan-asset, disease-level perspective.

GSK

Hybrid Permanent

Executive Regulatory Science & Strategy Director, Oncology

This role involves leading the Hematology group within Oncology Regulatory Affairs, providing strategic regulatory expertise and oversight for the development and commercialization of oncology products. Responsibilities include coaching regional and global regulatory leads, partnering with directors on innovative regulatory strategies, and representing the Global Regulatory Affairs function in senior interactions and health authority meetings.

AstraZeneca

On-site Permanent

Regulatory Affairs Intelligence Director

This role involves translating regulatory intelligence into strategic decisions that accelerate drug development and improve patient outcomes. You will work closely with senior leaders to anticipate regulatory shifts, shape external policy, and convert complex data into actionable insights.

AstraZeneca Cambridge, United Kingdom

On-site Permanent

Senior Director Clinical Operations Asset Lead - Hepatology, renal and cardiovascular disease

This role leads clinical operations for complex, high-impact assets in hepatology, renal, and cardiovascular disease, with responsibility for global Phase III trials, rare disease programmes, and co-development partnerships. The position involves setting operational strategy, managing CROs and vendors, driving data-led decision-making, and ensuring trial delivery to time, cost, and quality. It also includes direct leadership of clinical operations teams and integration of innovative trial methodologies.

GSK US$242,550 – US$404,250 pa

On-site Permanent

Senior Director Clinical Operations Asset Lead - Hepatology, renal and cardiovascular disease

This role leads clinical operations for high-complexity assets in hepatology, renal, and cardiovascular disease, with a focus on global Phase III outcomes trials, rare disease programmes, and co-development partnerships. The position drives operational strategy, risk management, and innovation in trial design, while managing senior vendor relationships and developing clinical teams. It emphasizes data-led decision-making, enterprise-wide impact, and compliance across a global development portfolio.

GSK US$242,550 – US$404,250 pa

On-site Permanent

SERM Associate Medical Director

This role involves providing medical and scientific expertise in safety evaluation and risk management for GSK's clinical and post-marketing assets. Responsibilities include signal detection, data analysis, and communication of safety risks, as well as supporting safety governance and cross-functional teams.

GSK United Kingdom

Hybrid Permanent

Regional Regulatory Manager

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.

GSK United Kingdom

Hybrid Permanent

Regional Regulatory Manager

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.

GSK

Hybrid Permanent

Regional Regulatory Manager

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.

GSK

Hybrid Permanent

Regional Regulatory Manager

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.

GSK

Hybrid Permanent

Global Study Manager

The Global Study Manager role involves leading the operational delivery of clinical studies from initiation to archiving, ensuring timelines, quality, and budget adherence. Key responsibilities include crafting delivery plans, leading the Operational Working Group, and collaborating with the Global Study Lead to achieve study deliverables. The role emphasizes innovation, risk management, and stakeholder communication.

GSK Stevenage, United Kingdom

Hybrid Permanent

Global Study Manager

The Global Study Manager role involves leading the operational delivery of clinical studies from initiation to archiving, ensuring timelines, quality, and budget are met. Key responsibilities include crafting delivery plans, leading the Operational Working Group, and collaborating with the Central Study Team to achieve study deliverables. The role emphasizes innovation, risk management, and stakeholder communication.

GSK United Kingdom

Hybrid Permanent

Global Study Manager

The Global Study Manager role involves leading the operational delivery of clinical studies from initiation to archiving, ensuring timelines, quality, and budget adherence. Key responsibilities include crafting delivery plans, leading the Operational Working Group, and ensuring compliance with ICH/GCP guidelines. The role emphasizes innovation, risk management, and stakeholder communication.

GSK

Hybrid Permanent

NIS P&D Project Management, Associate Director

The NIS P&D Project Management, Associate Director role involves developing and delivering Non-Interventional Studies (NIS) project plans, managing resources, and collaborating with various functional teams to ensure accurate and aligned project schedules. Key responsibilities include maintaining data quality in Planisware, forecasting costs, and managing risks.

GSK

Hybrid Permanent