Latest Pharmaceuticals Jobs

Head of Early Discovery

Your work will change lives. Including your own.The impact You'll MakeThe Head of Early Discovery will lead strategic initiatives to accelerate drug discovery by leveraging cutting-edge technologies, data-driven decision-making, and innovative scientific approaches. This role is pivotal in shaping Recursion’s...

Recursion United Kingdom

Senior Computational Biologist – Target ID

This role involves leading the integration of multi-omic and patient data to identify novel therapeutic targets at scale. The senior computational biologist will guide data science teams in building biologically grounded, semi-automated discovery pipelines, using advanced statistical methods to establish causal links between targets and patient outcomes. The position emphasizes translating complex biological data into actionable drug discovery insights with real-world impact.

Recursion United Kingdom US$151,800 – US$230,000 pa

Hybrid Permanent

Director, Oncology Clinical Biomarkers

This role involves developing and implementing biomarker strategies to support the clinical development of late-stage oncology assets. Responsibilities include collaborating with cross-functional teams, validating biomarker strategies, and integrating them into clinical plans to optimize decision-making and patient stratification.

GSK £189,750 – £316,250 pa

On-site Permanent

Director, Oncology Clinical Biomarkers

This role involves developing and implementing biomarker strategies to support the clinical development of late-stage oncology assets. Responsibilities include collaborating with cross-functional teams, validating biomarker strategies, and integrating them into clinical plans to optimize decision-making and patient stratification.

GSK United States £189,750 – £316,250 pa

On-site Permanent

Senior Scientific Engagement & Program Manager

This role involves planning and executing high-quality medical and scientific engagement activities across various therapeutic areas, including Oncology, Cardiovascular Disease, and Immunology. The Senior Scientific Engagement & Program Manager will coordinate advisory boards, congress activities, and medical education programs, ensuring seamless delivery and continuous improvement in processes and tools.

Novartis London, United Kingdom

Hybrid Permanent

Global Regulatory Affairs Associate Director (Cardio-Metabolic)

This role involves leading the development and submission of regulatory documents, providing strategic direction, and negotiating with health authorities to expedite approvals. The position also focuses on aligning regional regulatory approaches with global objectives and managing Health Authority interactions.

Novartis

Hybrid Permanent

(Fixed Term) Data Quality Control Specialist. Clinical Biomarker Laboratory

The Data QC Specialist will perform detailed quality control reviews of laboratory data and documentation to ensure accuracy, traceability, and compliance with regulatory standards. This role involves working closely with laboratory scientists and data management teams to resolve data discrepancies and maintain inspection readiness.

Moderna Oxford, United Kingdom

On-site Temporary

(Fixed Term) Data Quality Control Specialist. Clinical Biomarker Laboratory

The Data QC Specialist will perform detailed quality control reviews of laboratory data and documentation to ensure accuracy, traceability, and compliance with regulatory standards. This role involves working closely with laboratory scientists and data management teams to resolve discrepancies and maintain inspection readiness.

Moderna

On-site Temporary

Executive Regulatory Science & Strategy Director, Oncology

This role involves leading the Hematology group within Oncology Regulatory Affairs, providing strategic regulatory expertise and oversight for the development and commercialization of oncology products. Responsibilities include coaching regulatory leads, partnering on global strategies, and representing the function in senior interactions and health authority meetings.

AstraZeneca Canterbury, United Kingdom

On-site Permanent

Executive Regulatory Science & Strategy Director, Oncology

This role involves leading the Hematology group within Oncology Regulatory Affairs, providing strategic regulatory expertise and oversight for the development and commercialization of oncology products. Responsibilities include mentoring regulatory professionals, partnering with directors on global strategies, and representing the Global Regulatory Affairs function in senior interactions and health authority meetings.

AstraZeneca Cambridge, United Kingdom

On-site Permanent

Staff Platform Engineer, AI/ML Infrastructure

This role involves leading the technical strategy and architecture for AI/ML platform infrastructure, focusing on cloud platforms, CI/CD, observability, and security. The engineer will work closely with multiple teams to improve deployment reliability, scalability, and operational maturity of AI applications.

Pfizer London, SW7 2AP, United Kingdom

Hybrid Permanent

Staff Platform Engineer, AI/ML Infrastructure

The Staff Platform Engineer, AI/ML Infrastructure will lead the technical strategy for cloud platforms and AI/ML infrastructure, focusing on reliability, scalability, and security. Key responsibilities include architecting and operating scalable cloud platforms, defining reusable infrastructure patterns, and mentoring engineers to improve operational maturity across multiple teams.

Pfizer

On-site Permanent

VP, Medicine Development Leader - Respiratory

Leads global development of a respiratory medicine from clinical proof of concept through approval, serving as the primary accountable leader across a cross-functional matrix team. Defines strategic vision, drives evidence generation, lifecycle planning, and regulatory strategy while coordinating input from R&D, manufacturing, commercial, and regulatory stakeholders to deliver patient-focused therapies.

GSK US$309,750 – US$516,250 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