Latest Oncology Jobs

Statistics Director, Oncology

This role involves leading statistical strategies for key oncology programs, designing robust clinical trials, and mentoring statisticians. The position emphasizes innovation, regulatory interactions, and cross-functional collaboration to advance the development of new cancer therapies.

GSK Stevenage, United Kingdom

On-site Permanent

SERM Scientific Director, Oncology

The SERM Scientific Director role involves leading pharmacovigilance and risk management strategies for clinical development and post-marketing products. Responsibilities include evaluating safety data, managing safety concerns, and supporting regulatory activities. The role operates in a global, cross-functional environment and may include mentoring responsibilities.

GSK United Kingdom

Hybrid Permanent

Senior Scientist, Separation Sciences

Your work will change lives. Including your own.The Impact You’ll MakeWe are seeking a Senior Separation Scientist to join our Chemistry Automation team at our labs in Milton Park. In this primarily lab-based role, you will be responsible for maintaining...

Recursion Crathes, Alba / Scotland, 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

SERM Scientific Director

The SERM Scientific Director role involves leading pharmacovigilance and risk management planning, developing safety strategies, and ensuring the scientific soundness of data reviews. The position requires expertise in evaluating safety risks, managing cross-functional teams, and communicating safety issues to senior management.

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

Quality Validation and CSV Manager

The Quality Validation and CSV Manager will lead a team responsible for ensuring all validation activities, including process, cleaning, facility, and computer systems validation, comply with regulatory requirements and GSK quality standards. The role involves managing validation protocols, collaborating with cross-functional teams, and providing technical expertise and training.

GSK Barnard Castle, United Kingdom

On-site Permanent

Quality Manager (on Shift)

The Quality Manager on Shift ensures compliance with GMP and regulatory requirements during manufacturing and non-manufacturing activities. Key responsibilities include monitoring quality systems, investigating deviations, and supporting product release. The role involves working in a 24/5 shift pattern, including weekends, and promoting team collaboration and continuous improvement.

GSK East Hertfordshire, United Kingdom

On-site Permanent Shift-work

RTSM Project Manager

The RTSM Project Manager is responsible for the design, development, testing, and maintenance of clinical studies using the RAMOS IRT system. Key responsibilities include ensuring data integrity, configuring complex study designs, and driving continuous improvements in clinical supplies systems. The role involves technical oversight, problem-solving, and collaboration with cross-functional teams to enhance IRT processes and support clinical development.

GSK Stevenage, United Kingdom

Hybrid Permanent

Protein Engineering and Innovation Scientist

This role involves leading the development and deployment of advanced in-silico protein engineering and design principles to generate complex reagents for drug discovery. You will collaborate with computational experts, protein expression teams, and external partners to design, generate, and test engineered proteins, contributing to scientific innovation and project delivery.

GSK Stevenage, United Kingdom

Hybrid Permanent

Engineering Technician (numerous vacancies)

Engineering Technicians at GSK's Ware site support production activities and site operations by performing maintenance, calibration, and repair tasks on manufacturing and utility equipment. They work in a team to ensure safety, quality, and reliability, and may be involved in project work and continuous improvement initiatives.

GSK East Hertfordshire, United Kingdom

On-site Permanent Shift-work

Senior Technician

As a Senior Engineering Technician, you will lead the design, installation, and commissioning of new aseptic manufacturing equipment and facilities. You will work closely with project engineering, quality, and external vendors to ensure systems meet business, regulatory, and GMP requirements, and are ready for operational handover.

GSK Barnard Castle, United Kingdom

On-site Permanent

Audit Senior Lead (EMEA GMP Audit)

This role involves performing and managing GMP and compliance audits of Biopharm, Vaccines, and Pharmaceutical facilities. You will evaluate compliance with GMP, policies, and regulatory requirements, and provide subject matter expertise on sterile manufacturing. The role requires strong communication and influencing skills, and involves travel to various sites across the network.

GSK East Hertfordshire, United Kingdom

Hybrid Permanent

Audit Senior Lead (EMEA GMP Audit)

This role involves performing and managing GMP and compliance audits of GSK's Biopharm, Vaccines, and Pharmaceutical facilities across the EMEA region. You will evaluate compliance with GMP, regulatory requirements, and quality management systems, and provide subject matter expertise in sterile manufacturing. The role requires strong communication and influencing skills to engage with senior stakeholders and produce clear audit reports.

GSK Worthing, United Kingdom

Hybrid Permanent

Audit Senior Lead (EMEA GMP Audit)

The Audit Senior Lead role involves performing and managing GMP and compliance audits of GSK's Biopharm, Vaccines, and Pharmaceutical facilities. Responsibilities include evaluating compliance, conducting various types of audits, and producing clear audit reports to inform senior management of risks and corrective actions.

GSK Barnard Castle, United Kingdom

Hybrid Permanent