Biotechnology Jobs

• London
• Senior

Leads complex global and multi-regional clinical trials from start-up through close-out, with accountability for quality, timelines, budgets, regulatory compliance and sponsor objectives. Acts as primary strategic partner to sponsors and directs cross-functional teams across regions, with a focus on renal, obesity and MASH studies.

• 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
• Permanent

Provide scientific leadership across model evaluation and applied use cases, ensuring foundation models translate into real-world drug discovery and translational research workflows. Act as a senior individual contributor and key scientific partner, mentoring junior colleagues and working with Product and Business Development to turn biology and ML into customer-facing deliverables as the team scales.

• Reading
• Remote
• Director
• Permanent

Provides strategic medical and scientific subject matter expertise in obesity, cardiology, endocrinology or nephrology, leading proposal development and bid defence meetings as a medical director. Acts as a consultant across the research and development lifecycle and clinical trials, formulating clinical development plans and leading the strategic direction of a Center of Excellence. Requires a terminal MD degree and board certification, with occasional national or international travel.

• United Kingdom
• Remote
• Lead

Lead medical writer dedicated to a single client, authoring and reviewing clinical study reports, protocols, IBs, INDs and MAAs while advising on document strategy and regulatory requirements. Provides senior review, mentoring and training to junior writers and program managers, and leads process improvement initiatives. Therapeutic experience in neurology, immunology, oncology or vaccines is valued.

• United Kingdom
• Remote
• Senior

Clinical Research Associate role within PPD's Functional Service Provider division, dedicated to a client and embedded in multi-national project teams. You perform and coordinate all aspects of clinical monitoring, conducting monitoring activities independently across challenging projects. Requires ICH-GCP, EU and FDA knowledge, with award-winning training provided.

• Oxford
• Remote
• Mid-level

Owns the full sales cycle for Nanoimager microscopy systems across the UK and Nordic territory, from lead generation and tender-portal prospecting to demos and closing deals with academia, pharma and biotech customers. Maintains Salesforce pipeline and forecasting, feeds market insight back to Marketing and Customer Success, and travels at least 50% to customer sites.

Salesforce · Nanoimager

• Cambridge
• Hybrid · 3 days in office
• Director

Provides medical and scientific leadership across late-stage respiratory and immunology clinical programs, from Phase IIb to Phase IV. Involves designing, executing and interpreting pivotal trials, medical monitoring, regulatory document input and building relationships with external scientific experts in an international team.

• London
• Hybrid
• Director · manages people

Leads the global and US Medical Affairs Neuro-Oncology team, owning medical strategy, evidence generation and launch planning for pipeline and marketed assets. Serves as a key interface between Medical Affairs and R&D, clinical development and commercial functions, representing regional insights in governance forums. Combines people management with hands-on execution across a complex matrix.

• Sheffield
• Remote
• Senior

Leads research design and analytical strategies for clinical trials, developing and reviewing statistical analysis plans and authoring reports, abstracts and manuscripts. Acts as functional lead on study teams, directing biostatistical activities, performing complex analyses in SAS or R, and quality-controlling deliverables while mentoring junior staff and liaising with clients on scope and budget.

SAS · R

• Edinburgh
• Hybrid · 2–3 days in office
• £31,000 – £36,000 pa
• Mid-level
• Contract

Implement high-throughput plasmid assembly, colony PCR, Minipreps and pathway construction to build strains for hypothesis testing and model training. Work across disciplines in a lab-based, cross-pollinating team, with fortnightly research updates, mentorship and organised labbook/data keeping. Golden Gate assembly, Benchling in silico cloning and DNA sequencing are core.

Benchling · QIAgility

• Oxford
• On-site
• £40,000 pa
• Senior
• Permanent

Develops and optimises LC-MS workflows for low-input and single-cell proteomics and/or metabolomics, supporting researchers across the institute with experiment design, method development, data acquisition and interpretation. Works closely with bioinformatics, scientific computing and AI/ML teams, and helps build SOPs and training material for single-cell MS capability.

LC-MS · Flow Cytometry · Sequencing +5

• Maidenhead
• 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/FSPs and contributes to governance and development-plan decisions across therapeutic areas.

SAS · R

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

Leads the full scope of statistical contribution to a clinical development programme, defining statistical strategy and methodologies for trial design, analysis and regulatory submissions. Represents Biostatistics in interactions with authorities such as FDA, EMA and PMDA, and manages outsourcing or internal statistical programmers. Two positions support multiple therapeutic areas.

SAS · R