Latest Drug Discovery Jobs

SERM Scientific Director

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.

GSK

On-site Permanent

Senior Manager - CMC Regulatory Affairs Biopharm Development Projects

This role involves leading CMC regulatory activities for GSK's investigational, late development, and early commercial products. Responsibilities include driving CMC strategy, preparing regulatory documents, managing project activities, mentoring staff, and engaging with external agencies to ensure compliance and expedite submissions.

GSK Canterbury, United Kingdom

On-site Permanent

Senior Director, CFC CRM Lifecycle & Value Lead

This role involves managing the post-launch lifecycle of the CFC CRM platform across global markets, ensuring its stability, compliance, and continuous optimization. The Senior Director will work closely with various teams to prioritize market needs, manage configurations, and ensure successful adoption and value realization from CRM investments.

Pfizer

On-site Permanent

Clinical Development Medical Director (Associate Director)

This role involves overseeing medical and scientific aspects of clinical trials in Internal Medicine, including medical monitoring, safety data review, and clinical data management. The Medical Director will also contribute to protocol design, site selection, and investigator training, while mentoring others and ensuring data integrity and quality.

Pfizer Manchester, M1 4HD, United Kingdom

On-site Permanent

Senior Manager - CMC Regulatory Affairs Biopharm Development Projects

This role involves leading CMC regulatory activities for GSK's investigational, late development, and early commercial products. Responsibilities include driving CMC strategy, preparing regulatory documents, managing project activities, and mentoring staff. The position requires a strong understanding of regulatory requirements and the ability to communicate complex issues across departments and with external agencies.

GSK

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

NIS P&D Project Management, Associate Director

The NIS P&D Project Management, Associate Director is responsible for developing and delivering high-quality NIS Project Plans, managing resources, and collaborating with various functional teams to ensure alignment with R&D and marketed product portfolios. The role involves maintaining accurate project schedules, forecasting costs, and ensuring data quality in Planisware.

GSK

Hybrid Permanent