Latest Managed Services Jobs

Regional Regulatory Intelligence Manager

This role involves leading the regional regulatory intelligence strategy, ensuring alignment with global regulatory direction and Health Authority expectations. Responsibilities include identifying and translating regulatory intelligence into actionable insights, influencing regulatory outcomes, and driving cross-functional collaboration to embed intelligence into submission content and processes.

GSK

Hybrid Permanent

Regional Regulatory Manager

The Regional Regulatory Manager leads the development and execution of regional regulatory strategies for assigned assets, ensuring alignment with global goals and regional requirements. This role involves close collaboration with global and local teams, providing regulatory expertise, anticipating risks, and driving timely submissions and approvals.

GSK United Kingdom

Hybrid Permanent

Clinical Development Scientist, Manager

The Clinical Development Scientist (Manager) role involves providing scientific oversight and support for clinical trials in Internal Medicine. Responsibilities include protocol development, data review, safety monitoring, and contributing to clinical documents and reports. The role also involves collaborating with various stakeholders, including investigators, regulatory bodies, and safety review teams.

Pfizer

On-site Permanent

Senior Regulatory Associate

The Senior Regulatory Associate at Pfizer is responsible for managing regulatory activities for assigned products and markets, including new registrations, MA variations, and renewals. They will work closely with cross-functional teams, national regulatory authorities, and above-country hubs to ensure compliance and support clinical development activities.

Pfizer United Kingdom

Hybrid Permanent

SME - MSAT EM Technical Operations DS/DP

This role involves collaborating with internal and external stakeholders to support the commercial manufacture of large molecule drug substances and sterile drug products. Responsibilities include executing technical strategies, managing product lifecycle activities, and ensuring compliance with GMP standards. The role also involves supporting CMOs in audits, technical transfers, and continuous improvement initiatives.

GSK

On-site Permanent

Senior SME - MSAT EM Tech Ops DS DP

This role involves leading technical operations and providing strategic support for the commercial manufacture of large molecule drug substances and sterile drug products. Responsibilities include executing technical strategies, collaborating with external manufacturing partners, and ensuring compliance with GMP standards and continuous improvement initiatives.

GSK United States

On-site Permanent

Senior SME - MSAT EM Tech Ops DS DP

This role involves collaborating with internal and external stakeholders to support the commercial manufacture of large molecule drug substances and sterile drug products. Responsibilities include executing technical strategies, providing technical support, and ensuring compliance with GMP standards. The role also focuses on continuous improvement, change control, and managing critical lifecycle activities.

GSK

On-site Permanent

SERM Associate Medical Director

This role involves providing medical and scientific expertise in safety evaluation and risk management for GSK's clinical and post-marketing assets. Responsibilities include signal detection, data analysis, and communication of safety risks, as well as supporting safety governance and cross-functional teams.

GSK United Kingdom

Hybrid Permanent

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

This role involves planning and executing studies to generate robust health outcomes data for GSK's oncology products. The Director will collaborate with internal and external stakeholders to ensure evidence supports market positioning, reimbursement, and patient access. Key responsibilities include managing study timelines, ensuring deliverable quality, and translating customer needs into study concepts.

GSK United States

On-site Permanent

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

Regulatory Conformance Officer (12-month / Secondment)

As a Regulatory Conformance Officer, you will ensure that GSK's products meet all licensing and regulatory requirements, maintaining compliance with global market authorisations and supporting regulatory submissions. You will collaborate with multiple functions, including manufacturing, R&D, and global regulatory affairs, to deliver regulatory strategies and inspection readiness.

GSK Barnard Castle, United Kingdom

On-site Contract

Associate Director, Diagnostic Planning Lead - Oncology

Leads diagnostic planning activities within oncology translational medicine, coordinating cross-functional teams and external partners to advance diagnostic development programs. Oversees project timelines, regulatory documentation, budget management, and strategic alignment, with a focus on biomarker technologies and IVD development in support of oncology assets.

GSK Stevenage, United Kingdom US$151,500 – US$252,500 pa

Hybrid Permanent

Associate Director, Diagnostic Planning Lead - Oncology

This role involves leading diagnostic planning for oncology projects within GSK’s Translational Medicine team, coordinating cross-functional activities across clinical development, regulatory, and external partners. The Associate Director will manage timelines, budgets, and deliverables for diagnostic development programs, ensuring alignment with biomarker strategies and regulatory requirements. The position plays a key strategic role in advancing oncology assets through integrated project management and collaboration with diagnostics manufacturers and internal stakeholders.

GSK London, United Kingdom US$151,500 – US$252,500 pa

Hybrid Permanent

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 Stevenage, United Kingdom

Disease Area Lead - Hepatology, Renal and Cardiovascular diseases

Leads clinical operations strategy and delivery across Hepatology, Renal, and Cardiovascular disease portfolios within GSK’s R&D engine. Oversees end-to-end development from early phase through life-cycle management, driving operational excellence, team development, and cross-functional alignment. Champions data-driven decision-making, risk management, and innovation adoption to accelerate high-impact assets.

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

Hybrid Permanent