Latest Immunology Jobs

Clinical Development Medical Director - Cardiovascular

Lead clinical development for cardiovascular assets within GSK's Respiratory, Immunology & Inflammation Research Unit, driving translational and clinical strategies from early to late stages. Oversee study design, regulatory interactions, and cross-functional collaboration to deliver innovative medicines addressing unmet patient needs. Work in a hybrid model with significant scientific and strategic leadership responsibilities.

GSK £222,750 – £371,250 pa

Clinical Development Medical Director - Cardiovascular

This role involves leading clinical development for cardiovascular assets within GSK's Respiratory, Immunology & Inflammation Research Unit. The Medical Director will design and execute clinical development plans, provide medical oversight, and collaborate across functions to advance translational and clinical studies. The position emphasizes scientific leadership, regulatory engagement, and strategic input to bring innovative medicines to patients.

GSK

Hybrid Permanent

Director, Real World Data Strategy and External Partnerships Lead

This role involves leading the strategic execution of external data partnerships to enhance R&D and CPO activities. Responsibilities include defining and delivering RWD partnerships, maintaining data quality, and fostering relationships with academic institutions, health technology companies, and data holders to support regulatory approval and evidence generation.

GSK Stevenage, United Kingdom

Analytical Network Strategy Senior Director

This role involves developing and executing the analytical network strategy for GSK's supply chain, ensuring alignment with quality objectives. Responsibilities include defining QC testing principles, driving innovation in QC testing, and collaborating with cross-functional teams to integrate analytical testing into the end-to-end supply chain process.

GSK Stevenage, United Kingdom

Principal Scientist (m/f/d) Genomic Technologies, Human Genetics and Genomics

The Principal Scientist role involves working within GSK's Genomic Technologies team to develop and apply advanced methods for analyzing large-scale genetic and genomic data. Responsibilities include collaborating with multidisciplinary teams to identify causal genes, disease mechanisms, and potential drug targets, as well as contributing to the development of best-in-class analytical tools and methodologies.

GSK Stevenage, United Kingdom £74,250 – £202,125 pa

Senior Manager, Risk & Compliance Business Partners R&D

This role involves leading a team responsible for risk and compliance in GSK's R&D technology areas, providing hands-on consulting and assurance, and managing relationships with stakeholders. The position requires a deep understanding of cyber security, risk management, and compliance in a regulated environment.

GSK United Kingdom

Regulatory Affairs Manager, Oncology Therapeutic Group, Global Regulatory Affairs

Develop and execute global regulatory strategies for oncology assets, ensuring compliance and optimal labeling across markets. Collaborate with cross-functional teams and regulatory authorities to support product development and approvals. Drive innovation and process improvements within the regulatory lifecycle.

GSK United Kingdom €98,250 – €163,750 pa

Regulatory Affairs Manager, Oncology Therapeutic Group, Global Regulatory Affairs

Develop and execute global regulatory strategies for oncology assets, ensuring compliance and optimal labeling across regions. Collaborate with cross-functional teams to align regulatory plans with development goals and support submissions to health authorities. Focus on innovation, patient impact, and navigating complex regulatory landscapes in a hybrid working environment.

GSK €98,250 – €163,750 pa

Regulatory Affairs Manager, Oncology Therapeutic Group, Global Regulatory Affairs

Develop and execute global regulatory strategies for oncology assets, ensuring compliance and optimal product labeling across regions. Collaborate with cross-functional teams and regulatory authorities to support product development and approvals. Drive innovation and process improvements within the regulatory lifecycle.

GSK €98,250 – €163,750 pa

SERM Medical Director

This role involves leading pharmacovigilance and risk management strategy for GSK’s global pharmaceutical assets, with a focus on patient safety across clinical development and post-marketing phases. The Medical Director will lead safety governance, drive signal detection and risk mitigation, and represent GSK in regulatory discussions. It requires deep expertise in drug safety, cross-functional leadership in a matrix environment, and strategic input into global safety operations.

GSK United Kingdom

On-site Permanent

SERM Medical Director

Provides medical and scientific leadership in the safety evaluation and risk management of GSK’s oncology assets in clinical development. Interprets safety data, identifies and escalates safety signals, and delivers evidence-based recommendations to support benefit-risk decisions. Engages with global governance, regulatory authorities, and cross-functional teams to shape the safety profile of innovative oncology medicines.

GSK €119,250 – €198,750 pa

On-site Permanent

SERM Medical Director

Provides medical and scientific leadership in the safety evaluation and risk management of GSK’s oncology assets in clinical development. Interprets safety data, identifies and escalates safety signals, and delivers evidence-based recommendations to inform benefit-risk decisions. Engages with global cross-functional teams, regulatory authorities, and governance committees to shape the safety profile of innovative oncology medicines.

GSK €81,750 – €136,250 pa

SERM Medical Director

Provides medical and scientific leadership in the safety evaluation and risk management of GSK’s oncology assets in clinical development. Interprets safety data, identifies and escalates safety signals, and delivers evidence-based recommendations to inform benefit–risk decisions. Engages with global governance, regulatory authorities, and cross-functional teams to shape the safety profile of innovative oncology medicines.

GSK

Hybrid Permanent

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

Lead the design and execution of real-world evidence and health outcomes studies to support oncology assets, aligning scientific research with payer, clinician, and regulatory needs. Collaborate across medical, commercial, and R&D teams to generate robust data for value-based pricing and market access. Drive study planning, analysis, and dissemination while engaging external experts and shaping evidence strategies in a global context.

GSK £204,000 – £340,000 pa

On-site Permanent

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

This role involves planning, designing, and executing multiple real-world evidence studies to support the launch and market positioning of GSK's oncology products. The Director will collaborate with internal and external stakeholders to ensure the evidence meets the needs of payers, health systems, and providers, and will manage timelines, deliverables, and budgets.

GSK