Biotechnology Jobs

• London
• Director · manages people

Owns the strategy, organization and delivery of data and data science capabilities across R&D, leading a portfolio of R&D Data Categories through Senior Technical Data Product Owners. Sets governance and delivery standards while spending at least half the time hands-on writing code, building models and developing agentic AI systems for trusted data-science work.

OpenAI · CDISC SDTM · CDISC ADaM +2

• Stevenage
• On-site
• Mid-level
• Permanent

Designs, builds and maintains modular end-to-end data-flows across GSK's R&D division, integrating scattered systems and sources into reusable, machine-readable assets with compliance built into the pipeline. Combines hands-on coding and data specification work with coaching and peer review to raise the team's data-flow standards.

Azure · GCP

• Manchester
• Mid-level

Monitors clinical trial sites through selection, initiation, monitoring and close-out visits in line with GCP and ICH guidelines, while driving subject recruitment and tracking regulatory submissions, CRF completion and data queries. Works within a full-service, multi-sponsor site management team, training site staff and maintaining Trial Master File documentation.

• Reading
• Mid-level

Monitors Phase 3b and Phase 4 clinical trial sites across the UK and Ireland, performing selection, initiation, monitoring and close-out visits at a pace of 6-7 visits per month. The role involves driving subject recruitment, delivering protocol training, tracking regulatory submissions and CRF data, and maintaining Trial Master File documentation in line with GCP and ICH guidelines.

• 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

• Oxford
• On-site
• Mid-level
• Contract

Designs and delivers immunogenicity and bioanalytical strategies for regulated clinical programmes, developing ADA, nAb, PK and PD assays using ELISA, MSD and cell culture. Works with multidisciplinary teams to validate assays, manage reagents and SOPs, and integrate digital and AI-enabled tools. Site-based at Harwell within a growing mRNA-focused team.

ELISA · MSD · LIMS +2

• United Kingdom
• Remote
• Senior

Acts as independent Principal Investigator overseeing qualitative in-trial research studies, from design through delivery, for pharmaceutical clients. Applies methods like interviews and surveys to capture patient experience data, manages project budgets and timelines, and contributes to proposals and client development. Requires CAQDAS expertise and strong scientific writing.

Atlas.ti · NVivo · MAXQDA +1

• Leeds
• Director · manages people

Owns product strategy, roadmap and innovation for clinical pharmacology clinics and bioanalytical labs, spanning early-phase platforms like ClinSpark, LIMS/LIS, ELN, instrument connectivity and lab automation. Builds business cases and secures funding, governs a regulated portfolio, and leads multidisciplinary product teams and vendors across distributed sites.

ClinSpark · LIMS · LIS +7

• London
• Hybrid
• Senior
• Permanent

Drive innovation as a strategic consultant on high-impact drug discovery projects with external pharma and biotech partners. Navigate the full development pipeline from target discovery to patient stratification, applying statistical human genetics and large-scale genomic data analysis in R or Python. Partner-facing role translating complex findings into actionable insights.

• Oxford
• Hybrid
• Mid-level
• Permanent

Research Scientist role in the Molecular Simulations and Design team, combining generative models, physical simulation and experimental data to accelerate biomolecule design, initially enzymes. Involves developing methods such as Boltzmann samplers, long-timestep molecular dynamics, machine-learned interatomic potentials and flow matching/diffusion, with full-stack work from pre-training to design-build-test loops.

• Field Force (England / Wales)
• Hybrid
• £32,690 – £60,710 pa

Site-facing role managing Phase I–IV clinical trial sites, acting as the primary contact between the sponsor and sites. Responsibilities include site initiation visits, training, on-site and remote monitoring, risk assessment and mitigation, and closeout activities, working closely with cross-functional teams to ensure data integrity and compliance.

• Maidenhead
• Hybrid · 3 days in office
• Director · manages people

Leads scientific safety assessments for assigned medicinal products, partnering with Medical Safety Officers to prepare analyses and evaluations for regulatory compliance. Supports Safety Management Teams, conducts proactive safety data reviews, and serves as product point of contact, with hybrid working requiring three days on site.

Microsoft Word · Microsoft Excel · Microsoft PowerPoint

• Maidenhead
• Mid-level · manages people

Leads the preparation and finalisation of clinical documents within the Regulatory Medical Writing team, supporting the Immunology therapeutic area. Takes a lead role on assigned projects for content, scientific strategy, timing and tracking, and manages direct reports including hiring, goal-setting and development. Involves guiding cross-functional teams, peer review and maintaining knowledge of ICH and regulatory guidelines.

• Belfast
• £35,000 – £37,532 pa
• Entry level
• Contract

A graduate-level KTP Associate role based at Norbrook Laboratories, working within the R&D team to develop a data-driven framework for pharmaceutical scale-up of liquid dosage veterinary medicines. The project focuses on predictive modelling of process parameters and product quality across scales, combining chemical engineering principles with statistical and hybrid data modelling, delivered in collaboration with Queen's University Belfast's School of Pharmacy.

• Cambridge
• Hybrid · 3 days in office
• Director

Leads three mandates for an infectious disease portfolio: defining end-to-end publication strategy from target selection to clinical development, securing grants and partnerships with NGOs and philanthropic funders, and horizon-scanning emerging biotechnology. Partners with discovery, clinical, data and external academic stakeholders, coaching teams and influencing senior decision-makers.