Biotechnology Jobs

• United Kingdom
• Remote
• Director · manages people

Senior physician role providing metabolic therapeutic and drug-development expertise to a clinical research organisation, supporting major proposals and bid defences, client peer-to-peer engagement, and protocol design. Also trains and mentors internal clinical teams, authors regulatory documents, and liaises with investigators and KOLs. Requires an MD with metabolic subspecialty certification and fluency in English and Mandarin, with travel to China.

• United Kingdom
• Remote
• Director · manages people

Senior physician role leading medical science and strategy for oncology across a clinical research business, shaping RFP responses, bid defences and protocol design while engaging client medical leadership. Also provides therapeutic training, mentoring and regulatory document input, working in a matrixed global team with international travel.

• London
• Hybrid
• Director · manages people

Leads global operational delivery of early development oncology programs, managing Clinical Project Managers, Monitoring Leads and CTAs. Owns the clinical development plan, CRO and site selection strategy, budgets and timelines, and serves on Asset Teams. Requires deep first-in-human and Phase I oncology trial expertise.

Microsoft Office

• London
• Director · manages people

Lead global labelling strategy for assigned products across early and late-stage development, lifecycle management and marketed portfolios, serving as Therapeutic Area Lead. Drive core labelling documents including CCDS, USPI and EU PI, lead health authority negotiations, and shape a future USPI operating model while championing digitalisation and AI-enabled labelling solutions.

FDA · EMA · ICH

• 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

• London
• Hybrid
• €63,600 – €118,000 pa
• Lead · manages people

Lead and develop a team of Central Monitors while shaping risk-based monitoring strategies across a global clinical development portfolio. Oversee trial-data surveillance, signal detection and Key Risk Indicators, translating complex risk signals into actionable insights for Clinical Trial Teams. Works in a global matrix with clinical, data and risk-surveillance teams, driving continuous improvement through analytics and technology.

Artificial Intelligence

• Dublin, Ireland
• Hybrid
• €63,600 – €118,000 pa
• Lead · manages people

Lead and develop a team of Central Monitors while shaping risk-based monitoring strategies across a global clinical development portfolio. Oversee trial-data surveillance, signal detection and insight generation, translating complex risk signals into actionable insights and designing study-specific Key Risk Indicators and Quality Tolerance Limits.

Artificial Intelligence

• Oxford
• On-site
• Permanent

Designs and runs experiments on photosynthesis, carbon assimilation and yield-related pathways, using gas exchange, chlorophyll fluorescence and field work to assess plant physiology under varied conditions. Works in an interdisciplinary team on a stage-gated plant engineering programme, developing protocols and translating results into publications, IP and commercial opportunities.

• Oxford
• On-site
• Mid-level
• Permanent

Designs and runs evolution campaigns and selection schemes to optimise photosynthetic proteins, applying genome editing, directed evolution and protein engineering within a stage-gated plant engineering programme. Works in an interdisciplinary team translating photosynthesis, carbon fixation and yield findings into commercial and IP opportunities.

• Burgess Hill
• Hybrid
• £49 – £86 ph
• Lead
• Contract

Leads authoring, review and lifecycle management of clinical and performance evaluation documentation for a global diagnostics organisation, including protocols, study reports, investigator brochures and regulatory submissions. Works cross-functionally with regulatory, quality, R&D and medical affairs teams, conducting literature reviews and synthesising complex clinical data under IVDR and GCP.

AI-enabled tools

• Cambridge, United States
• Hybrid · 3 days in office
• Mid-level

First Technical Program Manager for the Drug Design and Medical Research function, supporting small molecule discovery programs in Cambridge and integrating with the London office. Responsibilities span program planning, timeline monitoring, risk reporting, budget forecasting and spend tracking, CRO and partner liaison, and embedding operational processes across teams.

Jira · Confluence

• London
• Hybrid
• US$189,750 – US$316,250 pa
• Director

Leads precision diagnostics strategy for oncology programmes, defining diagnostic requirements for trials and overseeing biomarker selection, assay validation and sample handling. Manages project plans, budgets and timelines while engaging diagnostic companies, clinical labs and vendors, and supporting regulatory submissions. Works cross-functionally with research, clinical, regulatory and commercial teams in a hybrid model.

FDA · EU IVDR · PMDA +2

• Stevenage
• Hybrid
• Director

Leads precision diagnostics strategy for oncology programmes, defining biomarker selection, assay validation and sample collection across multiple assets. Oversees project plans, budgets and regulatory submissions while managing external diagnostic partners and clinical labs. Hybrid role based in Stevenage, relocating to Cambridge by early 2029.

FDA · EU IVDR · PMDA/MHLW Japan +2

• Welwyn
• On-site
• Lead · manages people

Drives and facilitates efficient study start-up for Roche-sponsored clinical trials across the UK, developing start-up strategies and overseeing site activation and regulatory compliance. Engages with Ethics Boards, Health Authorities and CROs, manages budgets and contracts, and champions process automation and team development.

REC · MHRA · HRA

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

Lead all externalised drug discovery and preclinical lab operations, building and scaling a global CRO infrastructure for an AI-first drug design platform. Oversee experimental throughput, data QC and turnaround times, embed data-generation-by-design standards, and manage vendor governance, budgets and a team of CRO Scientific Leads, Operations Managers and Compound Managers.

AlphaFold · Agentic AI