Latest Pharmaceuticals Jobs

Director, Global Real-World Evidence & Health Outcomes Scientist, Oncology

This role involves planning and executing real-world evidence studies to support the launch and market positioning of GSK's oncology drugs. The Director will collaborate with internal and external stakeholders to ensure the generation of high-quality, scientifically credible evidence that meets regulatory and payer requirements.

GSK

On-site Permanent

Director, Global Strategic Insights – Oncology

This role involves leading the generation of strategic insights to shape the global product strategy for a key oncology brand in GSK's ADC portfolio. Responsibilities include driving commercial forecasts, conducting market research, and collaborating with cross-functional teams to ensure insights are integrated into business decisions and investment planning.

GSK United States

On-site Permanent

Sr. Scientist / APS, Data Compliance & Governance Management

This role focuses on enabling compliant cross-border data transfers for AstraZeneca’s Beijing AI Center by preparing scientific data for review, ensuring regulatory alignment, and streamlining processes. The candidate will triage data requests, assess compliance with regulations like DOJ EO 14117, trace data provenance, curate datasets, and coordinate with global stakeholders across R&D, privacy, and legal teams. The position bridges scientific data operations and governance to support AI-driven drug discovery while building scalable processes for future data sharing.

AstraZeneca Cambridge, United Kingdom

Hybrid Permanent

Executive Director Clinical Operations, Program Management

This role leads global clinical program delivery within AstraZeneca’s Oncology portfolio, focusing on strategic planning, operational excellence, and cross-functional leadership across late-stage development. The Executive Director will manage senior program directors, drive standardization, resolve escalated issues, and strengthen internal and external partnerships to accelerate patient impact. It involves governance, resource planning, financial stewardship, and leading organizational change in a dynamic, science-driven environment.

AstraZeneca Cambridge, United Kingdom

Hybrid Permanent

Director, Translational Science Lead

Leads translational science strategy for renal, inflammation, fibrosis, and neurodegeneration programs, driving biomarker development and validation from preclinical to clinical stages. Focuses on integrating multi-omics data, human assays, and novel technologies to inform clinical decision-making and patient stratification. Works across discovery and development to advance differentiated therapeutics through cross-functional collaboration and external partnerships.

GSK Canterbury, United Kingdom £178,200 – £297,000 pa

Hybrid Permanent

Programming Leader

The Programming Leader role involves overseeing project-level and study-level programming strategy and delivery for multiple complex studies in GSK's global pipeline. You will collaborate with cross-functional teams, ensure high-quality outputs, and champion the adoption of agile principles and new technologies to improve efficiency and data analysis.

GSK Stevenage, United Kingdom

Hybrid Permanent

Senior CMC Regulatory Strategy Manager

Leads CMC regulatory strategy for biopharmaceutical development and lifecycle management, coordinating submissions and ensuring compliance with global regulations. Works across cross-functional teams to address complex regulatory challenges and support continuous supply. Focuses on risk mitigation, process improvement, and influencing regulatory decisions in a matrix environment.

GSK Stevenage, United Kingdom €90,000 – €150,000 pa

Hybrid Permanent

Senior CMC Regulatory Strategy Manager

Leads CMC regulatory strategy for pharmaceutical development and lifecycle management, coordinating technical submissions and advising on global regulatory requirements. Works cross-functionally to ensure compliance, support inspections, and maintain product supply. Focuses on risk mitigation, process improvement, and influencing regulatory decisions across complex projects.

GSK London, United Kingdom £90,000 – £150,000 pa

Hybrid Permanent

MSAT Molecule Steward

This role involves providing end-to-end technical leadership for a pharmaceutical product throughout its lifecycle, from development to commercial manufacturing. The Molecule Steward ensures robust product control strategies, drives continuous process improvement, and coordinates technical strategy across drug substance, drug product, and analytical teams. The position requires deep scientific expertise, regulatory knowledge, and leadership in a matrixed global environment to maintain product quality and manufacturability.

GSK East Hertfordshire, United Kingdom €103,500 – €172,500 pa

Hybrid Permanent

Study Manager

The Study Manager role involves leading and coordinating clinical and evidence generation studies, working closely with internal and external teams to ensure studies are delivered on time, on budget, and in compliance with standards. Key responsibilities include monitoring study progress, drafting clinical documents, coordinating meetings, and managing study communications and budgets.

GSK Poland

Hybrid Permanent

Study Manager

The Study Manager role involves leading and coordinating clinical and evidence generation studies, working with study teams, vendors, and country colleagues to ensure studies are on time, on budget, and compliant with standards. Key responsibilities include monitoring study conduct, drafting clinical documents, coordinating meetings, and managing study communications and budgets.

GSK

Hybrid Permanent

Study Manager

The Study Manager role involves leading and coordinating clinical and evidence generation studies, working with study teams, vendors, and country colleagues to ensure studies are on time, on budget, and compliant with standards. Responsibilities include monitoring study progress, drafting key documents, coordinating meetings, managing communications, and overseeing clinical supplies and budget tracking.

GSK

Hybrid Permanent

Study Manager

The Study Manager role involves leading and coordinating clinical and evidence generation studies, working with study teams, vendors, and country colleagues to ensure studies are delivered on time, on budget, and compliant with standards. Key responsibilities include monitoring study progress, drafting clinical documents, coordinating meetings, managing study communications, and overseeing clinical supply and investigational product delivery.

GSK

Hybrid Permanent

Study Manager

The Study Manager role involves leading and coordinating clinical and evidence generation studies, working with study teams, vendors, and country colleagues to ensure studies are on time, on budget, and compliant with standards. Responsibilities include monitoring study progress, drafting key clinical documents, coordinating meetings, managing study communications, and overseeing clinical supply and investigational product delivery.

GSK

Hybrid Permanent

Study Manager

The Study Manager role involves leading and coordinating clinical and evidence generation studies, working with study teams, vendors, and country colleagues to ensure studies are delivered on time, on budget, and compliant with standards. Key responsibilities include monitoring study progress, drafting clinical documents, coordinating meetings, and managing study communications and budgets.

GSK

Hybrid Permanent