Biotechnology Jobs

• USA - Pennsylvania - Upper Providence
• Hybrid · 2 days in office
• US$189,750 – US$316,250 pa
• Director

Provides clinical and scientific leadership across translational and clinical studies within GSK's Respiratory, Immunology & Inflammation Research Unit, focusing on aging. Leads the Clinical Matrix Team, designs clinical development plans and protocols, oversees medical monitoring and safety, and drives regulatory interactions. Works cross-functionally with biology, regulatory, commercial and statistics to advance assets from early development.

• USA - Pennsylvania - Upper Providence
• On-site
• US$222,750 – US$371,250 pa
• Director

Serves as the physician within an oncology clinical programme team, leading medical monitoring and safety oversight for GI cancer studies. Interprets clinical and safety data, contributes to protocol development, and engages investigators, KEEs and health authorities. A core member of the Clinical Matrix Team, providing medical guidance within a matrixed pharma R&D environment.

AI-enabled insights

• Manchester
• Mid-level

Monitors oncology clinical trial sites through selection, initiation, monitoring and close-out visits, ensuring compliance with GCP and ICH guidelines. Tracks recruitment, regulatory submissions, CRF completion and data queries, and maintains Trial Master File documentation. Works within IQVIA UK's multi-sponsor Site Management team, with travel to sites required.

Trial Master File · Investigator's Site File

• Manchester
• Senior

Monitors clinical trial sites across selection, initiation, monitoring and close-out visits in line with GCP, while driving subject recruitment and tracking regulatory submissions, CRF completion and data query resolution. Also trains site staff, maintains TMF/ISF documentation and may support site financial management and start-up activities.

Microsoft Word · Microsoft Excel · Microsoft PowerPoint

• New York, United States
• Hybrid · 2–3 days in office
• US$124,400 – US$207,400 pa
• Lead · manages people

Leads the strategy, design and lifecycle management of Pfizer's clinical supply chain systems, aligning a 3-5 year product roadmap with Global Clinical Supply objectives. Partners with digital product managers and business SMEs on solution design, process improvement and portfolio prioritisation, reporting metrics to senior leadership. Hybrid role with up to 15% travel.

• Stevenage
• On-site
• Mid-level

Performs complex sample preparation and quantitative analysis of small molecules and biotherapeutics using instrumentation such as GC-MS, ICP-OES, HPLC and LC-MS, supporting both GMP and non-GMP stability studies. Works largely independently to set up, maintain and troubleshoot analytical instrumentation, interpret data for technical validity and compliance, and report results to client teams. Based full-time onsite at a pharmaceutical client site as part of a functional service provider partnership.

GC-MS · ICP-OES · HPLC +2

• Oxford
• Hybrid · 3–4 days in office
• Lead
• Permanent

Provides scientific and hands-on leadership for immunogenicity and ligand binding assay bioanalysis supporting mRNA-LNP therapeutic programs, spanning assay development, validation, clinical sample testing and regulatory submissions. Ensures GcLP compliance and partners with cross-functional teams, with opportunities to work alongside data and AI-enabled analytical approaches.

ECL · Gyrolabs · Reporter Gene Assays +3

• Exeter
• Entry level
• Contract

Computational PhD project using cell-free DNA sequencing to infer placental gene activity and dissect how genetic variants linked to adverse pregnancy outcomes affect placental function. The student develops tools to map nucleosomal footprints, integrates them with single-cell RNA-seq markers and GWAS summary statistics, and may generate new plasma data.

scRNA-seq · cfDNA Sequencing · GWAS

• United Kingdom
• £55,000 – £70,000 pa

This role involves leading in-vitro toxicology studies within a regulated preclinical environment, focusing on assay development and execution for product safety assessment. The scientist will apply advanced cell-based methods including Neutral Red, Ames, and micronucleus assays, interpret complex biological data, and support regulatory submissions. Collaboration with internal teams and external partners is key, alongside method validation and scientific reporting in a quality-assured laboratory setting.

• United Kingdom
• Remote
• Lead

Leads the design and implementation of bioanalytical strategies for a client-dedicated global biopharma team, ensuring lab-based activities align with context of use. Manages experimental design, tech transfer and regulatory submissions, interacting with lab scientists, cross-functional groups and Health Authorities in a matrix environment.

ddPCR · qPCR · RT-qPCR +6

• Opfikon, Switzerland
• Senior

Leads safety review and end-to-end signal detection across a product's lifecycle, using quantitative and qualitative methods alongside Global Safety Leads. Contributes to aggregate safety reports, risk management plans and regulatory responses, and mentors junior PVS staff. Works cross-functionally with Development, Medical Affairs and Regulatory teams on vaccine and national-significance products.

Microsoft Excel

• Maidenhead
• Mid-level

Oversees vendor delivery of medical evaluations for individual case safety reports, applying medical and scientific judgment on causality, expectedness and seriousness. Trains Medical Evaluators, sets assessment frameworks and drives process improvements across Global Safety and Pharmacovigilance. Requires deep pharmacovigilance knowledge and cross-functional stakeholder work.

• London
• Hybrid
• £56,511 – £104,949 pa
• Mid-level

Lead the development and maintenance of global labelling documents for neuroscience medicines, translating clinical and safety data into compliant product information. Facilitate cross-functional discussions, support Health Authority responses, and ensure timely implementation of labelling changes across global and major markets.

• Aylesbury
• £23 ph

Job summaryWe have an exciting opportunity for a Biomedical Scientist Microbiology at Buckinghamshire Healthcare NHS Trust to join the Microbiology Department at Stoke Mandeville Hospital. You will be responsible for performing specialist microbiology and serology investigations in accordance with departmental…

• Newcastle upon Tyne
• £21,805 pa
• Entry level
• Contract

Investigates the molecular mechanisms of liver dysfunction in childhood POLG-related mitochondrial disease, focusing on Alpers-Huttenlocher syndrome. Uses quantitative untargeted proteomics and immunohistochemistry on donated post-mortem liver tissue, and generates hepatic organoids from patient-derived iPSCs for disease modelling and therapeutic screening. Based in the Newcastle Mitochondrial Research Group with a placement at the University of St Andrews.

iPSCs