Latest Research Associate Jobs

Senior Research Associate, Bioanalytical & Molecular Assays - Ligand Binding Assays

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.

Moderna Oxford

Hybrid Permanent

Experienced Clinical Research Associate

Monitors clinical trial sites across selection, initiation, monitoring and close-out visits, ensuring compliance with GCP and ICH guidelines. Tracks recruitment, regulatory submissions, CRF completion and data queries, and maintains Trial Master File documentation. Works within a sponsor-dedicated team, liaising with sites and study team members.

IQVIA Reading

Senior Clinical Research Associate - FSP - South West England

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. Conducts onsite and remote monitoring visits, source data review and verification, and case report form review, while managing site quality risk assessments and maintaining CTMS and eTMF documentation. Works within a local study team supporting a key sponsor, with a focus on ICH GCP compliance, patient safety, and inspection readiness.

Parexel London

Remote

Senior Clinical Research Associate I/II - Sponsor Dedicated - Oncology Experience Needed

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.

Parexel London

Remote

Sr. Research Associate, Bioanalytical & Molecular Assays - Ligand Binding Assays

Develop, validate and run ligand-binding and cell-based bioanalytical assays generating pharmacodynamic and immunogenicity data for clinical mRNA programmes. Testing clinical samples in a GcLP-regulated lab using Thermo Watson LIMS, with documentation, SOPs and validation reports, partnering with Clinical Operations and Sample Management.

Moderna Clinical Development

Hybrid Permanent

CRA II, Oncology

Monitors oncology clinical trial sites through selection, initiation, monitoring and close-out visits, ensuring compliance with GCP and ICH guidelines. Tracks recruitment, regulatory submissions, CRF completion and data queries, and maintains Trial Master File documentation. Works within IQVIA UK's multi-sponsor Site Management team, with travel to sites required.

IQVIA Manchester

Assistant CRA

Supports clinical trial site management remotely, liaising with CRAs and study teams on site preparedness, document collection, vendor trackers and remote monitoring tasks. Handles essential documents, site payments, reconciliations and centralized monitoring reviews in line with SOPs and ICH GCP. Suits an early-career life sciences graduate seeking a UK-based remote clinical research role.

Thermo Fisher Scientific United Kingdom

Remote

CRA I/II/ Sr CRA - FSP - UK

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.

Thermo Fisher Scientific United Kingdom

Remote

Intern Clinical Operations

A 12-month clinical operations internship supporting trial setup, execution and closure across the UK, liaising with hospital sites and research staff and assisting with regulatory submissions and data monitoring. The intern collaborates with Clinical Research Associates and Start-Up Specialists and gains exposure to feasibility, patient recruitment and site management, working remotely with proximity to the Leeds headquarters.

Fortrea Maidenhead

Remote Internship

Vector Design Lead - Plant Biology Institute

Leads vector design strategy for gene edited and transgenic crop programmes, covering expression cassette architecture, guide RNA modules, donor templates and multiplex editing configurations. Owns the design-to-vector-release process, including construct QC, sequence management, vendor workflows and handover packages for transformation teams. Builds an industrial-grade vector design capability for corn, wheat and other strategic species, with SOPs, LIMS/ELN tracking and mentoring of scientists.

Ellison Institute of Technology Oxford

On-site Permanent

Genotyping and Event Delivery Manager - Plant Biology Institute

Leads the end-to-end event delivery workflow for gene edited and transgenic crops, from transformation output through sampling, molecular confirmation, QC review and handover. Designs and validates genotyping assays (PCR, qPCR, ddPCR, KASP, NGS) and builds stage-gate criteria, LIMS-enabled tracking and vendor strategies across corn and wheat programmes.

Ellison Institute of Technology Oxford

On-site Permanent

Postdoctoral Research Assistant in Biomedical Image Analysis

Develops cutting-edge machine learning and computer vision methods to analyse multi-omic and imaging data, identifying disease phenotypes and tissue architecture changes. Works with software engineers and data platform developers to translate research prototypes into robust, reproducible tools, bridging research and implementation.

University of Oxford Oxford £39,424 – £47,779 pa

On-site Contract

Associate Director (Scientific Data and Publications)

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, keeping published-information use copyright-compliant. Positions the portfolio for AI and text-mining exploitation, anticipating future licensing needs.

GSK Stevenage

Associate Director (Scientific Data and Publications)

Oversees 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 major information providers and connector across scientific, procurement, legal, copyright and technology teams, ensuring copyright-compliant use. Positions the portfolio for AI and text-mining exploitation, shaping future licensing needs.

GSK USA - Pennsylvania - Upper Providence

Lecturer / Associate Professor in Artificial Intelligence for Biomolecular Design & Molecular Interactions

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.

UCL London £68,284 – £76,244 pa

Hybrid Permanent