Latest Research Associate Jobs

Pfizer logo

Clinical Research Associate

This role involves managing and monitoring clinical trial sites to ensure compliance with Good Clinical Practice, patient safety, and Pfizer's standards. The Clinical Research Associate serves as the primary point of contact for investigator sites, conducts remote and on-site monitoring, supports patient recruitment, and resolves protocol and data issues throughout the trial lifecycle. The position requires close collaboration with study teams and site personnel, with significant travel expected across the UK and internationally.

Pfizer United Kingdom
Remote Permanent
Pfizer logo

Senior Clinical Research Associate I

This role involves managing and monitoring clinical trial sites to ensure compliance with protocols, patient safety, and data quality. The Senior Clinical Research Associate I serves as the primary point of contact for investigator sites, conducts on-site and remote monitoring, resolves protocol issues, and supports enrollment and database release. The position requires extensive knowledge of GCP, regulatory standards, and therapeutic areas such as oncology, with frequent travel expected.

Pfizer United Kingdom
Remote Permanent
Moderna logo

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

This role involves developing, validating, and executing ligand-binding and cell-based assays to support mRNA medicine development. The candidate will generate pharmacodynamic and immunogenicity data in a regulated GcLP environment, manage critical reagent characterization, and contribute to clinical sample testing using Watson LIMS. The position emphasizes scientific rigor, regulatory compliance, and collaboration within a high-performance team advancing novel bioanalytical assays.

Moderna Oxford, United Kingdom
Hybrid Permanent
Moderna logo

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

Develops and validates ligand-binding and cell-based assays to support clinical programs for mRNA medicines. Performs pharmacodynamic and immunogenicity testing in compliance with GcLP, using platforms like Thermo Watson LIMS. Contributes to assay development, reagent management, and regulatory documentation in a fast-paced, innovative lab environment.

Hybrid Permanent
AstraZeneca logo

Associate Principal Scientist, AI and Computational Tools, Oncology R&D (1-year

This role involves designing and deploying AI-powered tools and computational workflows to accelerate oncology drug discovery, with a focus on immuno-oncology. The scientist will build scalable data infrastructure, develop agentic AI and LLM-integrated solutions, and act as a technical leader across dry-lab and wet-lab teams. The position emphasizes translating complex biological data—such as single-cell and spatial transcriptomics—into reproducible, insight-generating systems while mentoring others in AI adoption and best practices.

AstraZeneca Cambridge, United Kingdom
On-site Contract
Autolus logo

Associate Director, Operational Intelligence

This role focuses on building advanced operational models and simulations to optimise Autolus' end-to-end processes across manufacturing, testing, supply chain, and quality. The individual will integrate data from multiple systems to create analytical frameworks that drive strategic decisions, improve capacity planning, and support business cases. It is a highly technical, insight-driven position requiring deep expertise in data modelling, cross-functional collaboration, and problem-solving in a regulated biopharmaceutical environment.

Autolus Stevenage, United Kingdom
On-site Permanent

Translational Medicine Expert – Dermatology, Associate Director

This role involves providing medical and scientific leadership in translational medicine for dermatology programs, spanning early to late-stage drug development. The expert will design and implement strategies for clinical pharmacology, biomarker development, and regulatory submissions, while leading cross-functional teams and supporting in-licensing opportunities. Work includes oversight of clinical studies, publication strategy, and engagement with regulatory and external stakeholders.

Novartis London, United Kingdom £67,900 – £126,100 pa
Hybrid Permanent

Global Clinical Operations AI Program Associate Director

Salary Range:£83,930.00 - £155,870.00Job Description Summary#LI-HybridLocation: WestworksRelocation Support: This role is based in London, Uk. Novartis is unable to offer relocation support; please only apply if accessible. Novartis is also unable to provide visa sponsorship for this position.This is a...

Novartis London, United Kingdom

Lecturer in Biomedical Science

Deliver high-quality teaching and research supervision on accredited undergraduate and postgraduate Biomedical Science programmes, with a focus on modules such as genetics, molecular pathology, blood sciences, and microbiology. Contribute to course development, student recruitment, and outreach while supporting student pastoral needs. Work within a dynamic academic team committed to enhancing the student experience through blended learning and practical laboratory instruction.

De Montfort University Leicester, Midlands Of England, United Kingdom £39 – £43 pa
Permanent

Laboratory Technician (Sensor Testing Laboratory)

This role involves supporting the day-to-day operation of a sensor testing laboratory, including equipment maintenance, inventory management, and adherence to safety and documentation protocols. The technician will assist scientists with research activities, conduct routine testing, and contribute to process improvements within a cutting-edge R&D environment focused on medical sensors. The position requires strong organisational skills, hands-on lab experience, and meticulous record-keeping.

Carbometrics Bristol, Bristol (county), United Kingdom £28,000 – £32,000 pa

Radiopharmaceutical QP

CMDO is Seeking to Appoint a Qualified Person. The Organisation is Engaged in Developing and Manufacturing New Medicines and Novel Formulations, Including a Wide Range of Oral Solid and Liquid Dosage Forms, Sterilised and Aseptically Filled Products, as well as...

CV-Library City of Westminster, Greater London
CSL logo

Director, Portfolio Development Process & Standards Lead

Lead the development and governance of processes, standards, and SOPs for CSL's global Portfolio Development function, ensuring high-quality clinical program execution. Drive cross-functional process improvement initiatives, change management, and training curriculum development. Collaborate with leadership and stakeholders across R&D to streamline decision-making and enhance operational excellence in a dynamic biotech environment.

CSL US$250,000 – US$280,000 pa
Hybrid Permanent
AstraZeneca logo

12 Month University Industrial Placement Student: Oncology DMPK

This 12-month industrial placement involves conducting DMPK bioanalysis and in vitro ADME studies to evaluate drug candidates in oncology. The role includes training in mass spectrometry, supporting pharmacokinetic research, and working within a cross-disciplinary matrix team across the UK and US. It offers hands-on experience in drug discovery within a leading biopharmaceutical R&D environment.

AstraZeneca Cambridge, United Kingdom £28,000 pa
GSK logo

Medical Director, Clinical Development, Hepatology

Lead clinical development activities for hepatology assets, contributing to clinical trial design, regulatory submissions, and cross-functional strategy. Work within project teams to advance drug development from early to registrational stages, ensuring scientific rigor and patient safety. Engage with regulators, external partners, and internal stakeholders to deliver transformative medicines for liver diseases.

GSK Stevenage, United Kingdom
GSK logo

Medical Director, Clinical Development, Hepatology

Lead clinical development activities for hepatology-focused drug programs, contributing to clinical trial design, regulatory submissions, and cross-functional strategy. Provide medical oversight and scientific leadership within project teams, ensuring patient safety and regulatory compliance. Engage with regulators, payors, and external experts to advance GSK’s pipeline in liver diseases.

GSK London, United Kingdom