Biotechnology Jobs

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

Medical Director - Oncology Clinical Development

The Medical Director, Oncology Clinical Development, will lead the design and execution of clinical trials for GSK's oncology portfolio, focusing on hematological malignancies. Key responsibilities include collaborating with multidisciplinary teams, ensuring patient safety, and contributing to regulatory submissions and publications.

GSK Stevenage, United Kingdom

Hybrid Permanent

Associate Director, Biostatistics (4)

The Associate Director (AD), Biostatistics, leads the full scope of statistical contribution to a clinicaldevelopment program. The AD provides statistical strategies for the clinical trials and regulatorysubmissions, and is accountable for the statistical deliverables within the program.Lead full scope of...

CSL

Director, Medical Evaluation & Case Processing Oversight

CSL's R&D organization is accelerating innovation to deliver greater impact for patients. With a project-led structure and a focus on collaboration, we’re building a future-ready team that thrives in dynamic biotech ecosystems. Joining CSL now means being part of an...

CSL

Senior Scientist, Bioconjugation

This role involves designing and conducting bioconjugation experiments to support oncology drug discovery, with a focus on conjugating small molecules to antibodies and related scaffolds. The scientist will characterise bioconjugates using HPLC, LC-MS, and other analytical techniques, optimise conjugation strategies, and contribute data-driven insights to early-stage research programmes. The position requires strong technical expertise in protein chemistry and robust laboratory practices within a collaborative, multidisciplinary environment.

AstraZeneca Cambridge, United Kingdom

On-site Permanent

Senior Scientist (Analytical, Bioscience Category)

This role involves developing and validating advanced analytical methods using LC-MS and HPLC to study antibody drug conjugates (ADCs) and linker payloads within oncology drug discovery. The scientist will work on bioanalytical assay design, support multi-disciplinary teams with data interpretation, and maintain compliance with GLP standards. The position emphasizes innovation in analytical science within a high-impact therapeutic context.

AstraZeneca Cambridge, United Kingdom

On-site Permanent

Associate Director, Global Regulatory Science, CMC

Lead global CMC regulatory strategy for mRNA medicines, guiding international submissions and ensuring compliance with health authority requirements. Collaborate with manufacturing and quality teams to support product development across vaccines, oncology, and rare diseases. Develop and maintain regulatory documentation in CTD format, while driving process improvements and change control assessments.

Moderna

Hybrid Permanent

Senior Project Specialist, Clinical Supplies

This role involves managing end-to-end clinical supply operations for Moderna’s mRNA-based therapies, ensuring investigational products are labeled, packaged, and distributed efficiently and in compliance with regulatory standards. The specialist coordinates with CROs, vendors, and internal teams to maintain supply chain continuity, troubleshoot logistics, and support digital innovation in supply systems, including AI-enabled tools and IRT platforms.

Moderna

Hybrid Permanent

Field Service Engineer - Stoke-on-Trent to Wrexham

As a Field Service Engineer, you will provide essential technical support for Roche’s medical diagnostic systems, ensuring seamless operation and maximum uptime. Your responsibilities include troubleshooting complex electro-mechanical faults, performing preventive maintenance, and training customers to use Roche’s diagnostic systems effectively.

Roche

On-site Permanent

Field Service Engineer - Stoke-on-Trent to Wrexham

As a Field Service Engineer, you will provide essential technical support for Roche’s medical diagnostic systems, ensuring seamless operation and maximum uptime. Your responsibilities include troubleshooting complex faults, performing preventive maintenance, and training customers on the use of Roche’s innovative diagnostic equipment.

Roche

On-site Permanent

Medical Director, ViiV Healthcare

The Medical Director role at ViiV Healthcare involves managing and reporting data from Phase 1-4 clinical trials, contributing to the design and medical governance of studies, and providing medical expertise and support throughout the trial process. The role is crucial in advancing HIV treatments and working closely with internal and external stakeholders to ensure the success of clinical studies.

GSK

On-site Permanent

Executive Director, Strategy, Oncology R&D

This role involves crafting and driving the global Oncology R&D strategy, integrating clinical, scientific, and commercial insights to shape portfolio priorities. You will advise senior leadership on complex strategic topics, optimize investment decisions, and collaborate across functions to deliver impactful patient outcomes.

AstraZeneca US$270,222 – US$405,332 pa

On-site Permanent

Senior Director, Head of Global Medical Governance, ViiV Healthcare

This role involves leading the global medical governance system at ViiV Healthcare, ensuring compliance and ethical standards across all medical activities. Responsibilities include developing and maintaining governance policies, advocating for medical governance, and collaborating with regional teams to embed best practices.

GSK United Kingdom

On-site Permanent

Head of RTSM (Randomization and Trial Supply Management)

This role involves leading the RTSM function in the US, partnering with clinical development, operations, quality, and external vendors to design and deliver patient-focused randomization and clinical supply solutions. Responsibilities include managing cross-functional teams, risk assessments, process improvements, and fostering collaboration across internal and external partners.

GSK United States

Hybrid Permanent

Senior Medical Director, Oncology Clinical Development - GU

This role involves leading clinical development for oncology assets, specifically in genitourinary (GU) cancers, within a global biopharma environment. The Senior Medical Director will design and execute phase 1-3 trials, ensure scientific integrity of data, and collaborate with internal teams and external experts to support regulatory filings and market launches. The position requires deep expertise in oncology drug development and strong leadership in a matrixed organization.

GSK PLN 593,250 – PLN 988,750 pa

Hybrid Permanent