Latest Recruitment Jobs

External Manufacturing DS Supply Director

This role leads the management of contract manufacturing organizations (CMOs) and supplier relationships to ensure reliable supply of drug substances, aligning with GSK's commercial and manufacturing strategies. The director oversees performance metrics, integrates new products into the supply chain, and drives operational excellence through governance, risk management, and team leadership. Collaboration with R&D and supply chain teams ensures timely delivery of medicines to patients.

GSK

On-site Permanent

External Manufacturing DS Supply Director

Lead the management of contract manufacturing organizations (CMOs) and supplier relationships to ensure reliable supply of medicines and vaccines. Oversee performance metrics, strategic alignment, and operational execution across a complex global supply chain. Provide leadership to teams and drive quality, efficiency, and innovation in external manufacturing operations.

GSK

On-site Permanent

Executive Director, Clinical Pharmacology/Pharmacometrics

This role involves leading clinical pharmacology and pharmacometrics strategies for rare disease and oncology programs, designing clinical studies, and interfacing with regulatory authorities. The position requires extensive experience in drug development, proficiency with modeling software, and collaboration with cross-functional teams.

Recursion United Kingdom

Senior AI Researcher

Work on cutting-edge AI research to accelerate drug discovery by developing models that bridge virtual cells and real-world data. Collaborate with interdisciplinary teams of scientists and engineers to translate complex biological data into scalable biomedical solutions. Focus on advancing end-to-end applications in discovery, design, and translation using large-scale datasets and frontier AI techniques.

Recursion United Kingdom

Associate Operator / Operator I

This hands-on manufacturing role involves executing production processes in a GMP cleanroom environment, operating cell-processing equipment, and maintaining cleanroom standards. The role supports continuous improvement and quality assurance, with a focus on delivering autologous cell therapy products.

Autolus Stevenage, United Kingdom

Materials Characterisation Team Undergraduate

This role involves hands-on laboratory work in materials characterisation, supporting the development and manufacture of medicines. You will plan and execute experiments, analyse data, and contribute to live projects, gaining valuable experience in a professional scientific environment.

Pfizer Sandwich, United Kingdom

Cell Therapy Account Executive (South UK)

The Cell Therapy Account Executive (CTAE) is responsible for developing and maintaining strong relationships with Advanced Therapy Treatment Centers (ATTCs) in the South UK. Key responsibilities include driving the utilization of Autolus' CAR T therapies, coordinating cross-functional activities, and ensuring a seamless customer experience. The role involves significant travel within the UK and requires deep clinical expertise in haematology and oncology.

Autolus United Kingdom

Undergraduate, Global Public-Private Partnerships

The role involves working with the Global Public-Private Partnerships (GP3) team at Pfizer, focusing on project management, communications, and reporting. Responsibilities include tracking project deliverables, managing project communications, and contributing to audit reports for the European Commission. The position offers opportunities to develop skills in project management, communication, and operations, with exposure to various departments and external partners.

Pfizer United Kingdom

Clinical Development Medical Director- Hepatology

Lead clinical development strategy and execution for hepatology assets within GSK’s R&D pipeline, driving early-phase programs from target identification through proof of concept. Provide medical oversight, design translational studies, and guide cross-functional teams to deliver innovative therapies for liver disease with a focus on scientific rigor and patient impact.

GSK

Hybrid 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 governance, regulatory authorities, and cross-functional teams to shape the safety profile of innovative oncology medicines.

GSK

Hybrid Permanent

Medical Director, Oncology Clinical Development - Lung & Head/Neck Cancers

The Medical Director, Oncology Clinical Development is responsible for providing medical expertise in the design, conduct, and interpretation of clinical studies for lung and head/neck cancers. Key responsibilities include medical monitoring, safety oversight, protocol development, and collaboration with cross-functional teams and external experts.

GSK United States £222,750 – £371,250 pa

Medical Director, Oncology Clinical Development - Lung & Head/Neck Cancers

The Medical Director, Oncology Clinical Development is responsible for providing medical expertise in the design, conduct, and interpretation of clinical studies for lung and head/neck cancers. This role involves leading medical monitoring, ensuring patient safety, and collaborating with cross-functional teams to integrate medical considerations into study execution and regulatory interactions.

GSK £222,750 – £371,250 pa

Medical Director, Oncology Clinical Development - Lung & Head/Neck Cancers

The Medical Director, Oncology Clinical Development role involves leading medical monitoring, safety oversight, and clinical data interpretation for clinical studies in lung and head/neck cancers. The role requires strong clinical expertise, collaboration with cross-functional teams, and engagement with external experts to ensure patient safety and study integrity.

GSK £222,750 – £371,250 pa

Medical Director, Oncology Clinical Development - Lung & Head/Neck Cancers

The Medical Director, Oncology Clinical Development is responsible for providing medical expertise in the design, conduct, and interpretation of clinical studies for lung and head/neck cancers. Key responsibilities include medical monitoring, safety oversight, and collaboration with cross-functional teams to ensure patient safety and clinical integrity.

GSK £222,750 – £371,250 pa

Medical Director, Oncology Clinical Development - Lung & Head/Neck Cancers

The Medical Director, Oncology Clinical Development is responsible for providing medical expertise in the design, conduct, and interpretation of clinical studies for lung and head/neck cancers. Key responsibilities include medical monitoring, safety oversight, and collaboration with cross-functional teams to ensure patient safety and clinical integrity.

GSK £222,750 – £371,250 pa