Latest IT Recruitment Jobs

Senior CMC Regulatory Strategy Manager

Leads CMC regulatory strategy for biopharmaceutical 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 shaping regulatory approaches and mentoring teams in a complex, science-driven environment.

GSK €90,000 – €150,000 pa

Hybrid Permanent

Senior CMC Regulatory Strategy Manager

Leads CMC regulatory strategy for biopharmaceutical 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 international environments.

GSK £144,375 – £240,625 pa

Hybrid Permanent

Small Molecule CMC Leader - Senior Director

Lead CMC strategy and execution for small molecule drug development from Phase 2 through commercialization, managing cross-functional teams and global regulatory filings. Oversee tech transfer, process scale-up, and lifecycle planning while ensuring compliance with US, EU, and international standards. Interface with senior leaders and health authorities to drive successful product launches and post-approval activities.

GSK

Hybrid Permanent

Director DDS Business Enablement & Implementation

This role involves leading high-impact transformation initiatives within Drug Development and Supply (DDS) at GSK, focusing on process optimization, organizational change, and performance enablement. The Director will act as a cross-functional integrator, driving strategic programs and ensuring adoption of new ways of working across a complex, matrixed biopharma environment.

GSK US$173,250 – US$288,750 pa

Hybrid Permanent

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

Privacy Lead – R&D / Chief Patient Office (CPO)

This role involves leading privacy strategy and compliance for R&D and patient-focused initiatives at GSK, ensuring responsible data use in clinical research, digital health, and AI-driven projects. The Privacy Lead embeds privacy-by-design principles, conducts risk assessments, and supports governance across highly regulated environments, balancing innovation with ethical data practices.

GSK

Hybrid Permanent

SERM Medical Director

The SERM Medical Director at GSK leads the safety evaluation and risk management of oncology assets in clinical development. Key responsibilities include interpreting safety data, managing safety signals, and providing expert medical input to support benefit-risk decisions. This role involves leading cross-functional teams, collaborating with regulatory authorities, and shaping the safety strategy for innovative oncology medicines.

GSK

On-site Permanent

Head, Oncology Clinical Development - ADCs

The Head, Oncology Clinical Development- ADCs, will report to the SVP, Head of Oncology Clinical Development. The role holder will be accountable for the design and implementation of the clinical development strategy across a particular asset across multiple tumor types...

GSK United States

Head, Oncology Clinical Development - ADCs

The Head, Oncology Clinical Development- ADCs, will report to the SVP, Head of Oncology Clinical Development. The role holder will be accountable for the design and implementation of the clinical development strategy across a particular asset across multiple tumor types...

GSK

Head, Oncology Clinical Development - ADCs

The Head, Oncology Clinical Development- ADCs, will report to the SVP, Head of Oncology Clinical Development. The role holder will be accountable for the design and implementation of the clinical development strategy across a particular asset across multiple tumor types...

GSK

Head, Oncology Clinical Development - ADCs

The Head, Oncology Clinical Development- ADCs, will report to the SVP, Head of Oncology Clinical Development. The role holder will be accountable for the design and implementation of the clinical development strategy across a particular asset across multiple tumor types...

GSK

Medical Director, Clinical Development, Immunology

We are seeking a Medical Director, Clinical Development, Immunology for a clinical program in food allergy. The Medical Director, Clinical Development, Immunology will support the Clinical Development Lead (CDL) and clinical team to plan and execute a clinical program, consisting...

GSK United States

Medical Director, Clinical Development, Immunology

We are seeking a Medical Director, Clinical Development, Immunology for a clinical program in food allergy. The Medical Director, Clinical Development, Immunology will support the Clinical Development Lead (CDL) and clinical team to plan and execute a clinical program, consisting...

GSK

Medical Director, Clinical Development, Immunology

We are seeking a Medical Director, Clinical Development, Immunology for a clinical program in food allergy. The Medical Director, Clinical Development, Immunology will support the Clinical Development Lead (CDL) and clinical team to plan and execute a clinical program, consisting...

GSK

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