Biotechnology Jobs

• London
• Remote
• Mid-level
• Permanent

Lead site performance and compliance for assigned clinical protocols across the South East, acting as primary site contact through all study phases. Conduct remote and on-site monitoring to ICH/GCP standards, manage regulatory documentation in CTMS and eTMF, and mentor junior CRAs. Involves roughly 65-75% domestic and international travel.

CTMS · eTMF · MS Office

• 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.

• 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)

• Leeds
• Hybrid
• Senior
• Permanent

On-site CRA role monitoring Phase I–Ib studies inside a 100-bed Leeds Clinical Research Unit, covering pre-study, initiation, routine monitoring and close-out visits. Works alongside clinic, pharmacy and lab teams during first-in-human dosing days, using integrated eSource and EDC systems to focus on data integrity and protocol compliance rather than mechanical SDV.

eSource · EDC

• 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

• London
• Remote
• Senior

Responsible for the successful delivery of clinical studies at assigned investigator sites, acting as the primary point of contact for site management, monitoring, and study execution. Leads site preparation, initiation, routine monitoring, and close-out, conducting onsite and remote visits, source data review and verification, and CRF review while managing risk-based quality and regulatory compliance. Works within a local study team supporting a key sponsor, with travel across the UK and internationally.

CTMS · eTMF

• 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.

• United Kingdom
• Remote
• Mid-level

Independently manages basic project tasks including budgets, timelines and client correspondence, while supporting protocol and report development under senior supervision. Conducts qualitative data collection such as cognitive interviews and focus groups, performs literature reviews and data analysis, and assists with scientific publications. Requires 10-30% travel and works within a multidisciplinary patient-centered research team.

Microsoft Word · PowerPoint · Excel +5

• United Kingdom
• Remote
• Entry level

Supports patient-centered research projects by conducting literature reviews, cognitive interviews and focus groups, managing data collection and coding, and assisting with analysis and reporting. Works within a multidisciplinary team spanning psychometrics, epidemiology and health sciences, with some independent project task management.

MS Word · PowerPoint · Excel +7

• 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

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

Lead the design, assembly and clinical validation of a novel dialyser prototype within the Thermofluids Group, testing with blood-mimicking fluids and human blood to assess cleaning efficiency, clotting risk and biocompatibility. Work alongside two other Research Associates covering numerical simulation and experimental fluid dynamics, in collaboration with the Medical School and Sheffield Teaching Hospitals.

• 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

• 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

• London
• Hybrid
• £50,733 – £59,484 pa
• Mid-level
• Contract

Lead the harmonisation, integration and analysis of large-scale multi-omics datasets including single-cell transcriptomics, epigenomics and proteomics, building reproducible Nextflow or Snakemake pipelines on HPC or cloud infrastructure. Work with AI and mathematical modelling teams within a multidisciplinary consortium spanning Imperial, UCL and industry partners on an ARIA-funded programme studying innate immune protection against respiratory viral infections.

Nextflow · Snakemake · Unix +3

• Sheffield
• £39,560 – £41,885 pa
• Entry level
• Contract

Contribute to a research programme analysing explanted polymeric medical devices, investigating how implant degradation, tissue responses and patient-specific factors drive complications. Establish experimental and sample-handling workflows, develop lab methods to characterise tissue and immune responses, and collaborate with academic, clinical, regulatory and patient partners including Sheffield Teaching Hospitals and Cambridge.