Latest Project Services Jobs

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Statistics Leader / Associate Director of Statistics

GSK Oncology is committed to discovering and developing new therapies with the potential to change the lives of patients with cancer. The Oncology Clinical Development Statistics group is seeking exceptionally talented Statisticians to provide end-to-end statistical leadership across oncology evidence...

GSK
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Statistics Leader / Associate Director of Statistics

GSK Oncology is committed to discovering and developing new therapies with the potential to change the lives of patients with cancer. The Oncology Clinical Development Statistics group is seeking exceptionally talented Statisticians to provide end-to-end statistical leadership across oncology evidence...

GSK
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Research Scientist – FTE - Pharmaceutical Sciences (PS)

AstraZeneca is a global, science-driven biopharmaceutical company dedicated to discovering, developing and delivering innovative, meaningful medicines and healthcare solutions that enrich the lives of patients. Here you are encouraged and supported to think creatively in our dynamic environment, free from...

AstraZeneca Macclesfield, United Kingdom
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Health Economics Manager

Job Title: Health Economics ManagerLocation: Pancras Square, LondonCompetitive salary and benefitsAbout the RoleWe are seeking an experienced Health Economics Manager to lead the development and delivery of health economic strategies and evidence that demonstrate the value of innovative therapies and...

AstraZeneca London, United Kingdom
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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
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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
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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
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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
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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
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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
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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
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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
GSK logo

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
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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
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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