Biotechnology Jobs

• Oxford
• Hybrid
• Senior

Perform bioanalytical assays using molecular and cellular techniques such as ddPCR, qPCR, RT-qPCR and gel electrophoresis to quantify RNA in biological matrices. Support phase-appropriate assay development, qualification and validation within a GCLP-compliant clinical framework, partnering with internal and external labs and cross-functional teams. The role blends basic science research, bioanalysis and clinical development, with exposure to digital and automation tools.

Droplet Digital PCR · qPCR · RT-qPCR +2

• 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.

• Harrow
• Remote
• Senior

Monitors clinical trial sites across the UK as the sole point of contact, conducting qualification, initiation, monitoring and termination visits and producing visit reports. Manages site quality, regulatory documentation and drug accountability while developing recruitment strategies to meet enrolment timelines. Fully decentralised role with less travel and a lower protocol load than industry peers.

Clinical Trial Management System · Electronic Document Management System · Excel +1

• Oxford
• Hybrid · 3–4 days in office
• Senior
• Permanent

Develops, validates and runs ligand-binding and cell-based bioanalytical assays generating pharmacodynamic and immunogenicity data for clinical mRNA programmes. Works in a GcLP-regulated lab using Thermo Watson LIMS and electronic notebooks, handling clinical samples, critical reagents, SOPs and validation reports while partnering with Clinical Operations and Sample Management.

Thermo Watson LIMS · Watson LIMS · LabVantage eLBN +1

• Reading
• Mid-level

Conducts site qualification, initiation, monitoring and close-out visits for a pharmaceutical sponsor as an embedded member of IQVIA's Clinical Functional Service Partnership team. Monitors patient safety, data integrity and protocol compliance, mentors junior staff, and travels up to 40-60% of the time within the region.

Investigator Site Files (ISF) · Trial Master Files (TMF)

• London
• Remote
• Senior

Lead monitoring activities for assigned oncology clinical trial sites, from site activation through closeout, conducting both onsite and remote visits, source data verification and regulatory document oversight. Partner with a dedicated sponsor in an FSP model, driving enrollment, resolving protocol deviations and supporting audit readiness. Requires at least five years of oncology clinical research experience and up to 75% travel.

CTMS · EDC

• Maidenhead
• Mid-level

Unblinded monitoring of pharmacies at clinical trial sites across Scotland and the North of England, with possible additional UK and Ireland sites. Involves Investigational Product oversight, ICH-GCP compliance, eTMF documentation and acting as primary contact for pharmacy monitoring, within a sponsor-dedicated team.

eTMF

• Keele
• £39,560 – £48,337 pa
• Entry level
• Contract

A postdoctoral research associate role delivering the insect-focused laboratory components of a consortium project on a planthopper-vectored bacterial plant disease. The postholder investigates vector ecology and transmission biology using insect rearing, bioassays, EPG analysis and molecular techniques such as PCR and qRT-PCR, with occasional travel within the UK and Europe.

Electrical Penetration Graph · Bioinformatics

• 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.

• Glasgow
• £39,906 – £46,049 pa
• Entry level
• Contract

Develops high-throughput Python workflows to analyse coarse-grained molecular-dynamics simulations of engineered protein assemblies, extracting geometric, topological and structural descriptors such as curvature, lumen dimensions and packing order. Builds structure-property relationships and reusable, version-controlled pipelines feeding predictive and active-learning models, within an interdisciplinary team spanning computational chemistry, machine learning, protein science and engineering.

Martini · GROMACS · VMD +2

• London
• Hybrid
• £68,284 – £76,244 pa
• Senior
• Permanent

Develops and leads an AI-driven research programme in biomolecular design and molecular interactions, spanning protein-ligand, protein-protein and protein-nucleic acid systems. Combines structural biology, biophysics, quantitative biology and machine learning, while teaching computational biology and biomolecular design at undergraduate and postgraduate level, including a new MRes in AI for Bioscience.

• Oxford
• On-site
• £40,178 – £48,700 pa
• Entry level
• Contract

Conducts research characterising crosslinked proteins and lipids under a Wellcome Trust-funded grant, using proteome and lipidome methods including sample preparation, LCMS and data analysis. Manages project administration, guides junior researchers and students, and contributes to reports, publications and external seminars.

LC-MS · nanoLC-MS

• Stevenage
• Director

Accountable for GSK R&D's enterprise portfolio of external scientific content and data licenses, managing budget, forecasting, cost controls and vendor commercial terms. Acts as senior interface to information providers and connector across scientific, procurement, legal, copyright and technology teams, ensuring copyright-compliant use and positioning content for AI and text-mining exploitation.

Excel · PowerPoint · Word +2

• USA - Pennsylvania - Upper Providence
• Director

Accountable for GSK R&D's enterprise portfolio of external scientific content and data licenses, including budget, forecasting, cost controls and retiring under-used sources. Manages vendor relationships and commercial terms, maintains copyright-compliant governance and user guidance, and works across scientific, procurement, legal, digital and technology teams to make licensed content AI- and text-mining-ready.

Excel · PowerPoint · Word +2

• 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