Biotechnology Jobs

• London
• Hybrid · 2 days in office
• US$340,500 – US$567,500 pa
• Senior · manages people

Leads global development of a cancer vaccine asset from late-stage transition through approval and launch, acting as single point of accountability and chairing a cross-functional matrix Medicine Development Team spanning clinical, translational, regulatory, manufacturing and commercial. Drives strategy, go/no-go decisions and lifecycle plans for novel vaccine platforms such as mRNA and neoantigen-based therapies.

mRNA · Checkpoint Inhibitors

• Waltham, United States
• Hybrid · 2 days in office
• US$340,500 – US$567,500 pa
• Director · manages people

Leads global development of a cancer vaccine asset from late-stage transition through approval and launch, acting as single point of accountability across major markets. Builds and directs a matrix Medicine Development Team spanning clinical development, immunology/biomarkers, manufacturing, regulatory, safety, medical affairs and commercial, and represents the asset to senior governance boards.

mRNA · Personalized Vaccine Manufacturing · Checkpoint Inhibitors

• Reading
• Senior

Monitors clinical trial sites across the UK, handling selection, initiation, monitoring and close-out visits in line with GCP and ICH guidelines. Manages multiple protocols, drives subject recruitment, tracks regulatory submissions and CRF data, and maintains Trial Master File documentation. Based in Reading with regular travel to investigative sites.

• Reading
• Mid-level

Monitors clinical trial sites across 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 a sponsor-dedicated team, liaising with sites and study team members.

• United Kingdom
• Remote
• Senior · manages people

Accountable for delivering clean clinical data on time and within contract for low-to-moderate complexity haematology/oncology trials, managing operational and quality aspects in line with ICH GCP. Develops monitoring plans, CRF documents and Trial Master File content, tracks timelines and metrics, and may handle start-up, ethics submissions and project financials. Works within a team of CTMs, with travel to sites and a focus on radiopharmaceuticals, cell & gene therapy and CAR-T studies.

Outlook · Excel · Word

• Opfikon, Switzerland
• Hybrid · 3 days in office
• US$212,000 – US$251,000 pa
• Director

Leads the full statistical contribution to a clinical development programme, defining statistical strategy for trial design, analysis and regulatory submissions, and representing Biostatistics in interactions with the FDA, EMA and PMDA. Also manages outsourcing to CROs and internal statistical programmers, and supports departmental improvement initiatives.

SAS · R

• 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

• Oxford
• On-site
• Senior

Sole-contributor scientist role developing and executing biochemical and molecular biology assays for PK/PD analysis, spanning genomic DNA/RNA isolation, qPCR, ddPCR, RNA sequencing, MSD, ELISA and immunoblotting. Works within Moderna's Clinical Bioanalytical team at Harwell, Oxfordshire, ensuring GcLP-compliant assay qualification and validation, troubleshooting with external CRO partners, and building internal and external mRNA-based bioanalytical capability.

MSD · LIMS · eLNB +1

• Sheffield
• Remote
• Senior

Lead research design and analytical strategies for clinical trials, developing and reviewing statistical analysis plans and authoring reports, abstracts and manuscripts. Direct biostatistical activities as functional lead within a study team, overseeing quality control of deliverables and mentoring junior staff. Uses SAS and R in a global, matrixed, remote-working team.

SAS · R

• Harrow
• Remote
• Senior

Senior regulatory affairs consultant role focused on CMC writing and variations strategy for vaccines and biological products. You will draft CMC sections and scientific rationales for submissions, coordinate activities across multiple projects, liaise with global affiliates and manufacturing sites, and manage client relationships on a dedicated project without people-management duties. Work is home or office based across various European locations.

FDA · EMA · MHRA

• 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
• On-site
• £55,000 – £70,000 pa
• Senior

Lead and execute in-vitro regulatory and genetic toxicology studies, developing and applying Neutral Red, Ames and micronucleus assays within a quality-assured laboratory. Provide technical direction across pre-clinical research, product development and regulatory programmes, collaborating with multidisciplinary teams and external CROs and academic partners.

OECD Guidelines · ECVAM · ICCVAM +3

• United Kingdom
• Remote
• Senior

Monitors investigator sites using a risk-based approach, conducting remote and on-site visits to assess protocol and regulatory compliance, performing SDR, SDV and CRF review, and documenting findings in reports. Acts as a site processes specialist ensuring trials follow ICH-GCP, applicable regulations and SOPs, while developing collaborative relationships with investigational sites and supporting audit readiness.

CTMS · Microsoft Office

• Maidenhead
• Senior

Lead and manage clinical trial sites across a diverse portfolio spanning oncology, neuroscience, cell & gene and CAR-T therapies. The role emphasises patient safety, data integrity and building trusted relationships with investigators, with autonomy and support for complex, innovative study designs.

• Maidenhead
• Mid-level

Monitors clinical trial sites across a diverse portfolio spanning oncology, neuroscience, general medicine, cell & gene and CAR-T therapy. Leads site management, builds relationships with investigators and study teams, and safeguards patient safety and data integrity on complex, first-in-class studies. Distinct for its breadth across therapeutic areas and advanced therapy exposure rather than a narrow single-indication focus.