Latest IT Consulting Jobs

Senior CMC Regulatory Strategy Manager

Leads CMC regulatory strategy for biopharmaceutical development and lifecycle management, ensuring compliance with global regulations and supporting submissions, inspections, and supply continuity. Works cross-functionally to shape regulatory approaches and mentor teams, with a focus on innovation and risk mitigation in complex regulatory environments.

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 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 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

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 Clinical Operations Asset Lead - Hepatology, renal and cardiovascular disease

This role leads clinical operations for high-impact, complex global trials in hepatology, renal, and cardiovascular disease, with a focus on late-phase outcomes studies and rare diseases. The position shapes operational strategy, drives innovation in trial design, and ensures delivery across a diverse asset portfolio. It involves leading vendor partnerships, managing regulatory and quality compliance, and developing clinical teams within a patient-ambitious, data-driven environment.

GSK Stevenage, United Kingdom US$242,550 – US$404,250 pa

Hybrid Permanent

Senior Director, Structured Component Management (SCM) Strategy, Operations & Governance

This role leads the design and governance of structured component management (SCM) standards across R&D at GSK, ensuring compliance with regulatory requirements and enabling audit-ready, AI-compatible content. The Senior Director will establish component taxonomy, metadata schemas, lifecycle governance, and drive adoption across global teams. It involves close collaboration with Medical Writing, Regulatory, Quality, and Data Governance to scale automated and generative authoring workflows in a regulated environment.

GSK Stevenage, United Kingdom

Hybrid 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

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

This role leads clinical operations for complex, multi-indication assets in hepatology, renal, and cardiovascular disease, with strategic oversight of global Phase III trials, rare disease programmes, and co-development partnerships. The position involves shaping operational strategy, managing high-level vendor relationships, and driving innovation in trial design including decentralised and hybrid models. It requires leadership in risk management, data-driven decision-making, and team development within a global regulatory and compliance framework.

GSK United Kingdom US$242,550 – US$404,250 pa

On-site Permanent