Biotechnology Jobs

• London
• Hybrid · 2 days in office
• US$189,750 – US$316,250 pa
• Director · manages people

Provides clinical and scientific leadership across early-phase clinical development programs in GSK's Respiratory, Immunology & Inflammation Research Unit, with a focus on aging research. Leads a Clinical Matrix Team, designs clinical development plans and study protocols, oversees medical monitoring and safety, and represents programs in regulatory interactions. Works cross-functionally with biology, translational sciences, commercial, regulatory and statistics partners.

• USA - Pennsylvania - Upper Providence
• Hybrid · 2 days in office
• US$284,625 – US$474,375 pa
• Director · manages people

Leads clinical development medical activities for cardiovascular programs across early and later phase studies, shaping clinical development plans, study designs and translational strategies. Provides medical monitoring and safety oversight, serves as clinical point of contact with regulators and investigators, and leads a cross-functional clinical matrix team within the Cardiovascular Medicine group. Requires a medical degree, board certification in cardiovascular medicine and at least five years of clinical research experience.

• Oxford
• On-site
• Permanent

Builds computational tools and data analysis pipelines for plant biology, working at the intersection of multi-omic analysis and software development. Integrates transcriptomics, metabolomics, proteomics and imaging data, developing pipelines for image segmentation, feature extraction and phenotyping, and preparing datasets for agentic workflows. Collaborates closely with bioinformaticians, research scientists and AI engineers in the Bioinformatics platform team.

• Oxford
• On-site
• Entry level
• Permanent

Supports the smooth operation of research laboratories through cleaning, equipment maintenance, calibration and inventory management of reagents and consumables. Acts as point of contact for external servicing visits, handles and transports biological samples, and helps maintain health and safety compliance including waste disposal and temperature-sensitive storage.

• London
• Hybrid · 3 days in office
• Lead

Technically lead the Platform group, owning cloud infrastructure and the software lifecycle for training and inference systems. Work across GCP, Kubernetes, Docker and Terraform with scientists and ML researchers, reporting to the Director of Engineering in a small, fast-moving team.

GCP · Kubernetes · Docker +7

• London
• Hybrid · 3 days in office
• Mid-level

Join a newly formed Scheduling team to own and extend systems orchestrating compute allocation for complex ML workloads on Kubernetes. You'll design scheduling policies like gang scheduling and topology-aware placement, build custom Kubernetes controllers and CRDs, and optimize GPU/TPU utilization while partnering with ML researchers on reliability and SLOs.

Kubernetes · Kueue · Volcano +4

• London
• Remote
• Senior · manages people

Leads cross-functional clinical trial teams for biotech clients, owning project plans, budgets, P&L, risk management and client relationships from Phase I to III. Requires strong CRO experience and therapeutic expertise in oncology plus areas such as dermatology, women's health, neurology, rare disease or radiopharmaceuticals, working fully remotely within a select EMEA country.

Microsoft Excel · PowerPoint · Microsoft Word +1

• Sheffield
• Remote
• Lead

Configures, tests and maintains electronic Clinical Outcome Assessment studies in platforms such as Medidata Designer eCOA, translating protocols and licensed instrument requirements into questionnaires, schedules and branching logic. Acts as technical contact for sponsors and vendors, coordinates eCOA-to-EDC integration and deployment, and mentors less-experienced study designers across multiple global trials.

Medidata Designer eCOA · Medidata Rave

• 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

• Uxbridge
• Director · manages people

Owns the clinical strategy for one or more neuropsychiatry programs, serving as Clinical Trial Physician and clinical point of accountability for the Clinical Development Team. Leads trial design, data interpretation, regulatory submissions and health authority interactions, with matrix leadership across global scientific teams.

• Leeds
• Hybrid
• Entry level
• Internship

A student placement supporting the Clinical Operations team in day-to-day coordination of clinical studies, including maintaining the Trial Master File (TMF/eTMF), tracking activities in CTMS, generating reports and distributing study supplies. Based in Leeds with flexibility to work remotely, though onsite working is preferred and may be required.

TMF · eTMF · CTMS +4

• High Wycombe
• Hybrid · 3 days in office
• Entry level
• Internship

A 12-week summer internship in EMEA Global Regulatory Affairs within the Oncology therapeutic area, working on a hybrid model with three days on site. Interns join a global matrixed team supporting clinical strategies and Phase I-III oncology studies, contributing to regulatory strategy, clinical trial applications and product registration activities, with a mentor, cross-functional team meetings and a research poster presented at a company-wide symposium.

Microsoft Outlook · Microsoft Excel · Microsoft PowerPoint +5

• Cambridge
• £71,200 – £113,200 pa
• Senior · manages people

Leads day-to-day operations of a genomics hub, managing NGS workflows such as RNAseq, ATACseq and single cell genomics, plus SOPs, data management, equipment and budgets. Provides hands-on wet lab guidance and acts as subject matter expert on experimental design while training and supervising technical staff.

• Reading
• Mid-level

Conducts site monitoring visits including selection, initiation, monitoring and close-out, ensuring compliance with GCP and ICH guidelines. Manages site recruitment plans, protocol training, regulatory submissions and data query resolution, maintaining Trial Master File documentation. Focused on oncology studies within a biotech-focused clinical research team.

Microsoft Word · Microsoft Excel · Microsoft PowerPoint

• Uxbridge
• Director

Serves as primary medical accountability for multiple Phase 1-3 clinical trials in GI oncology, leading medical data review, safety assessment and site interactions within a Study Delivery Team. Partners with Clinical Scientists on protocol design, benefit/risk analysis and health authority interactions, while building relationships with principal investigators and thought leaders.