Biotechnology Jobs

• Waltham, United States
• Hybrid
• US$123,000 – US$205,000 pa
• Lead

Owns operational delivery of diagnostics across early and late-stage oncology trials, from biosample collection and clinical trial assays at reference and central labs to audit-ready data. Works in a matrix with Diagnostic Strategy, Biomarker, Clinical Operations, Data Management, Regulatory, Quality and Procurement, plus external CROs, labs and vendors, and mentors colleagues as a subject matter expert.

CRO

• Stevenage
• Hybrid

Predominantly laboratory-based role planning, executing and interpreting LC-MS and LC-MS/MS experiments to characterise biopharmaceutical molecules. You will develop and troubleshoot analytical methods, investigate product quality attributes and post-translational modifications, and support early-phase programmes through forced degradation and comparability studies. Works across Discovery and CMC Development teams, with hybrid working available.

Protein Metrics · JMP · SIMCA

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

Lead and develop a team of Central Monitors, shaping central and site monitoring strategies across a global development portfolio. Oversee trial-data surveillance, risk reviews and signal detection using Central Monitoring technology, translating complex risk signals into actionable insights for Clinical Trial Teams. Partners with clinical, data and risk-surveillance teams to strengthen risk-based monitoring and Risk-Based Quality Management.

Artificial Intelligence

• London
• Hybrid
• Senior

Plans and executes medical and scientific engagement activities such as advisory boards, congress symposia, external expert engagements and medical education programmes across oncology, cardiovascular, renal, neuroscience and immunology. Works within the International Medical Affairs Center of Excellence, translating engagement strategy into operational plans, managing vendors, logistics and budgets, and reinforcing compliant, audit-ready ways of working.

CRM Software

• Cambridge
• Director
• Permanent · Flexible

A senior scientific leadership role shaping and delivering a drug discovery strategy, driving adoption of AI-assisted design, predictive modelling, automation and computational science across a diverse portfolio. The post-holder mentors multidisciplinary teams spanning biology, chemistry, protein design, pharmacology and translational sciences, and acts as a scientific ambassador in client engagements, proposals and partnerships.

• Cambridge
• Senior

Acts as subject matter expert for stem cell culture technologies, leading development, optimisation and delivery of cellular systems for drug discovery. Manages multiple cell culture programmes, supplies high-quality cell batches for high-throughput screening, and troubleshoots assays while ensuring biological safety compliance. Collaborates with multidisciplinary teams and external partners across global sites.

Automated Liquid Handling Platforms · High-Throughput Screening

• Slough
• On-site
• Senior
• Permanent

Performs routine, non-routine and stability testing of biologic drug substances using ELISA, cell-based potency assays and Biacore (SPR), while coordinating assay activities and managing project priorities and timelines. Acts as a technical subject matter expert, mentoring colleagues and supporting method development, validation, troubleshooting and GMP-compliant documentation within a client-facing analytical service department.

ELISA · Biacore · Vi-CELL +2

• Wrexham
• Hybrid
• Lead
• Permanent

Leads Cell Line Development and Upstream Process Development strategies for biologic products, from candidate selection through commercial manufacturing. Acts as subject matter expert within cross-functional CMC teams, managing CDMO partnerships, supporting regulatory submissions and technology transfer, and mentoring junior scientists.

CHO

• London
• Hybrid
• Mid-level

Leads global cross-functional teams to plan, coordinate and deliver regulatory submissions for new marketing authorisations, new indications and other major filings. Manages integrated submission timelines, scenario planning, risk mitigation and forecasts, working with Regulatory Affairs, Clinical, Quality and Manufacturing under the CTD/eCTD framework.

RIMS

• London
• Hybrid
• Director · manages people

Leads the development and execution of international regulatory strategy across European and Rest of World markets, from first-in-human through post-marketing. Represents Global Regulatory Affairs on core development teams, manages project plans and resources, and advises senior management. Also a people manager within the International GRA leadership team, driving process improvement and regulatory policy engagement.

EMA

• Macclesfield
• On-site
• Senior
• Permanent

Designs and executes work plans for early drug discovery projects within a Protein Sciences team, supporting multiple projects and presenting results to clients. Hands-on role focused on recombinant protein expression using insect cell systems such as BEVS, S2 and Sf9, including construct design, baculovirus generation and troubleshooting difficult targets like membrane proteins.

BEVS · Sf9 · Sf21 +2

• Leeds
• Hybrid
• Senior
• Permanent

Leads data management activities across early phase trials, including healthy volunteer and patient populations, multi-site studies and reduced timelines. Accountable for all DM deliverables, resource allocation, client relationships and scope changes, while mentoring the internal study team and adopting new DM technologies.

• Maidenhead
• Hybrid
• Senior

Leads clinical data management for one or more oncology studies within a sponsor-dedicated (FSP) model, acting as the primary client contact from study set-up through close-out. Combines strategic oversight of vendors, budgets and CDM deliverables with hands-on work such as eCRF design and data cleaning, collaborating with data coordinators and statistical programmers.

eCRF

• Gaithersburg, United States
• On-site
• US$218,330 – US$327,494 pa
• Director

Leads competitive intelligence for AstraZeneca's oncology R&D, owning delivery of clinical and commercial analysis that shapes therapy-area strategy and portfolio investment decisions. Works with a specialist team and senior leadership, translating complex data into insights and challenge. Requires oncology, clinical or investment analysis background.

• Cambridge, United States
• On-site
• US$218,330 – US$327,494 pa
• Director

Leads competitive intelligence for AstraZeneca's oncology pipeline, delivering clinical and commercial analysis that shapes therapy-area strategy and investment decisions. Partners with senior leadership and cross-functional teams, providing respectful challenge and insight into the evolving oncology landscape. Requires oncology, clinical research or investment analysis background with strong communication and influence skills.