Latest Research Associate Jobs

Senior Research Associate, Bioanalytical & Molecular Assays

This role involves developing, qualifying, and validating molecular bioanalytical assays—such as qPCR, ddPCR, and RT-qPCR—to support clinical pharmacokinetic and pharmacodynamic studies within a GCLp-compliant environment. The scientist will work closely with cross-functional teams to ensure robust data generation, maintain regulatory compliance, and integrate emerging digital and automation technologies into workflows. A strong focus on reagent management, assay documentation, and continuous process improvement is central to the position.

Moderna Oxford, United Kingdom

Hybrid Permanent

Senior Research Associate, Bioanalytical & Molecular Assays

This role involves developing, optimizing, and validating molecular bioanalytical assays—such as qPCR, ddPCR, and RNA isolation—to support mRNA-based clinical programs. The scientist will work within GCL0-compliant (GCLP) frameworks to generate pharmacokinetic and pharmacodynamic data, ensuring regulatory compliance and data integrity. Collaboration with cross-functional teams and adoption of digital tools and automation are key to advancing clinical trial execution and analytical processes.

Moderna

Hybrid Permanent

Postdoctoral Research Associate (Proteomics and Metabolomics)

Conduct integrated proteomic and metabolomic analysis of aqueous humour samples from glaucoma patients using mass spectrometry and computational methods. Process low-volume biological samples, perform quantitative data analysis, and integrate multi-omics datasets. Contribute to manuscript writing, conference presentations, and public communication of findings as part of a multidisciplinary research team.

University of Liverpool Liverpool, Northern England, United Kingdom £39 pa

Contract

Post-doctoral Research Associate (Molecular Microbiologist)

This role involves conducting molecular microbiology research to understand how Neisseria gonorrhoeae evades innate immune defences. The researcher will work within Dr. Lavender’s group on a funded project focusing on bacterial pathogenesis and host–pathogen interactions. Key responsibilities include experimental design, data generation, and contributing to a deeper understanding of immune evasion mechanisms in a highly antibiotic-resistant pathogen.

University of Liverpool Liverpool, Northern England, United Kingdom £39 – £46 pa

Contract

Associate Director, PBPK-PD Translational Modeling, DMPK

Lead the development and application of mechanistic PBPK-PD models for oligonucleotide therapeutics and antibody-drug conjugates, translating preclinical data into clinical predictions. Integrate AI-enabled and QSP approaches to support human dose projection, candidate selection, and PK/PD strategy across discovery and early development. Collaborate with multidisciplinary teams to embed model-informed drug development into project workflows.

GSK Stevenage, United Kingdom

Hybrid Permanent

Associate Director, PBPK-PD Translational Modeling, DMPK

Associate Director, PBPK-PD Translational Modeling, DMPKDrug Metabolism and Pharmacokinetics (DMPK) | Research & Development GSK.Closing Date: 1st September 2026 (COB)Business IntroductionAt GSK, we have bold ambitions for patients, aiming to positively impact the health of 2.5 billion people by the...

GSK

Associate Principal Scientist - In Vivo Pharmacology (Kidney or Metabolic)

Lead the design and execution of in vivo pharmacology studies within kidney or metabolic disease research, providing scientific leadership on client-sponsored drug discovery programmes. Work closely with multidisciplinary teams and clients to develop study strategies, interpret complex data, and mentor junior scientists. This role offers broad exposure to innovative therapeutics across biotech and pharma pipelines in a scientifically driven CRO environment.

Mackie Myers Ng11Gr, United Kingdom £45,000 – £55,000 pa

Associate Director, R&D Project Management

Leads the operational delivery of high-impact, global R&D projects within a cross-functional biotech environment. Focuses on strategic planning, budget and timeline management, risk mitigation, and stakeholder reporting. Provides mentorship to junior project management staff and ensures robust project execution across drug research, development, and manufacturing.

CSL

Hybrid Permanent

Hourly Paid Associate Lecturer in Biotechnology

Deliver high-quality, research-informed teaching across Foundation, BSc, and MSc Biotechnology programmes, supporting student development through lectures, practical sessions, and assessments. Contribute to programme administration and enhancement within an inclusive, student-centred learning environment. Work as part of a collaborative academic team with strong industry and NHS links.

Liverpool John Moores University Liverpool, Northern England, United Kingdom £53 ph

On-site Contract Part-time

Associate Director, Safety Epidemiology – Global Patient Safety

Lead the design and execution of post-authorisation safety studies using real-world data to assess and communicate the safety profiles of AstraZeneca’s medicines. Provide strategic epidemiological input to regulatory submissions, safety signal evaluations, and diversity initiatives, collaborating with internal teams and external partners. Drive methodological excellence in pharmacoepidemiology and contribute to global patient safety decision-making across a broad product portfolio.

AstraZeneca Chatham, ME4 4NP, 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

Postdoctoral Scientist in Molecular Biology of Neoantigen pMHC-TCR Interactions in Sarcoma

This role involves conducting molecular research on neoantigen prediction, TCR selection, and pMHC-TCR interactions in sarcoma, with a focus on chromosomal translocation-derived neoantigens. The postdoctoral scientist will develop and apply techniques in protein expression, surface plasmon resonance, and T-cell reporter assays to advance the scientific foundation for personalised TCR therapies. The position requires independent research, collaboration within a multidisciplinary team, and dissemination of findings through publications and scientific presentations.

University of Oxford Oxford, South East England, United Kingdom £40 pa

Contract

Global Development Lead, Internal Medicine, Sr. Director (MD)

Leads clinical development for assigned assets in Internal Medicine, serving as the primary clinical accountability point within Pfizer's Research & Development. Designs and oversees global clinical trials, regulatory submissions, and cross-functional team coordination, with potential involvement in obesity-related late-stage programs. Engages with external stakeholders and ensures compliance with scientific, regulatory, and safety standards.

Pfizer England

On-site Permanent

Global Development Lead, Internal Medicine, Sr. Director (non-MD)

This role involves leading clinical development for Internal Medicine assets within Pfizer's Research & Development division, with a focus on obesity-related therapies. The Global Development Lead will design and oversee global clinical trials, create development plans, and ensure regulatory compliance across regions including China and Japan. The position requires cross-functional leadership, engagement with external stakeholders, and contribution to regulatory submissions and product labeling.

Pfizer England £214,900 – £358,100 pa

On-site Permanent

*Senior Clinical Development Medical Director - Renal

Leads the end-to-end clinical development strategy for renal programs, from early through registrational phases. Provides medical leadership across trial design, regulatory documentation, and safety oversight. Works cross-functionally to translate data into clinical and regulatory pathways, ensuring robust benefit-risk decision-making throughout the program lifecycle.

Novartis London, United Kingdom

On-site Permanent