Latest Research Associate Jobs

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

The Global Development Lead (GDL) is responsible for leading the clinical development of assigned assets in Internal Medicine. This involves designing and executing clinical trials, creating development plans, and ensuring regulatory compliance. The role also includes collaborating with cross-functional teams, providing expert input on clinical data, and engaging with external stakeholders to drive strategic insights.

Pfizer

On-site Permanent

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

The Global Development Lead (GDL) is responsible for leading the clinical development of assigned assets in Internal Medicine. This involves designing and executing clinical trials, creating development plans, and collaborating with cross-functional teams to ensure regulatory submissions and product approvals globally. The role also includes providing expert input on trial design, regulatory activities, and engaging with external stakeholders to drive strategic insights.

Pfizer

On-site Permanent

Senior Medical Director, Oncology Clinical Development - GU

This role involves leading clinical development activities for GSK’s oncology portfolio, with a focus on genitourinary (GU) cancers. The Senior Medical Director will design and oversee phase 1–3 clinical trials, ensure scientific integrity, and collaborate with internal teams and external experts to advance drug development. The position plays a key role in regulatory submissions, lifecycle management, and shaping clinical strategy in a global, matrixed environment.

GSK Stevenage, United Kingdom US$284,250 – US$473,750 pa

Hybrid Permanent

Senior Medical Director, Oncology Clinical Development - GU

This role involves leading clinical development for genitourinary (GU) oncology programs within GSK’s pipeline, with responsibility for designing and executing phase 1–3 trials, ensuring scientific integrity, and supporting regulatory submissions. The Senior Medical Director will collaborate across functions and represent GSK externally with key experts and at medical meetings, driving data generation and strategic input for innovative oncology therapies.

GSK £284,250 – £473,750 pa

Hybrid Permanent

Senior Scientist, Translational PKPD

As a Senior Scientist in Translational PKPD Modeling & DMPK, you will apply your expertise in PKPD modeling and simulation to advance cancer biology understanding and accelerate drug discovery. You will provide specialist modeling input into pre-clinical projects, develop PKPD models, predict human dosing, and contribute to early clinical trials. This role involves cross-functional collaboration, strategic decision-making, and enhancing AstraZeneca’s translational research through publications and presentations.

AstraZeneca Cambridge, United Kingdom

On-site Permanent

Executive Regulatory Science & Strategy Director, Oncology

This role involves leading the Hematology group within Oncology Regulatory Affairs, providing strategic regulatory expertise and oversight for the development and commercialization of oncology products. Responsibilities include coaching regulatory leads, partnering on global strategies, and representing the function in senior interactions and health authority meetings.

AstraZeneca Canterbury, United Kingdom

On-site Permanent

Technical Program Coordinator, DDMR, London

As a Technical Program Coordinator, you will support the Drug Design and Medical Research (DDMR) function by managing program planning, monitoring timelines, tracking actions, and reporting risks. You will work closely with drug design teams, internal stakeholders, and external partners to ensure effective communication and alignment across the organization.

Isomorphic Labs London, United Kingdom

On-site Permanent

Director of Engineering (ML Platform), London

This role involves leading the strategic direction and operational excellence of the Platform teams, which enable the training and serving of large-scale AI models in biotech. Responsibilities include defining the long-term vision, mentoring a diverse team, and ensuring robust, scalable, and developer-friendly services across multiple disciplines.

Isomorphic Labs London, United Kingdom

On-site Permanent

Machine Learning Scientist - Quantum Chemistry

This role involves developing machine learning models grounded in quantum chemistry to accelerate small-molecule drug discovery. You will create synthetic datasets using quantum mechanics, build scalable and reproducible ML pipelines, and collaborate with computational and experimental scientists to model molecular energetics and protein–ligand interactions. The work directly feeds into molecular design tools used across Roche, with opportunities to publish, present, and contribute to open-source.

Roche Welwyn Hatfield, United Kingdom

Hybrid Permanent

Machine Learning Scientist - Small Molecule Drug Design

Develop and apply machine learning models to accelerate small-molecule drug discovery with a focus on protein–ligand interactions, binding affinity, and molecular properties. Collaborate closely with computational chemists, structural biologists, and experimental researchers to validate and refine ML-generated hypotheses. Contribute to scientific impact through publications, open-source contributions, and conference engagement.

Roche Welwyn Hatfield, United Kingdom

Hybrid Permanent

Principal Scientist, Bioanalytical & Molecular Assays

This role involves leading the development and validation of advanced molecular assays such as RT-qPCR, dPCR, and NGS to support clinical biomarker strategies across Moderna’s therapeutic pipeline. The scientist will work hands-on in assay design, optimization, and data interpretation, ensuring compliance with GCLP standards while integrating genomics, bioinformatics, and clinical insights. Collaboration with cross-functional teams is key to translating molecular data into actionable decisions for drug development.

Moderna Oxford, United Kingdom

Hybrid Permanent

Director, CMC Regulatory Affairs

Lead the development and execution of CMC regulatory strategy for small molecule drugs in global clinical trials and marketing applications. Author and manage high-quality regulatory submissions across the US, EU, and rest of world, while advising cross-functional teams on compliance, risk mitigation, and regulatory best practices. Support clinical trial materials and GMP inspections, ensuring alignment with evolving global regulations.

Recursion North Tyneside, NE29 8EP, United Kingdom £207,500 – £280,720 pa

Remote Permanent

Director, Regulatory Affairs

This role involves leading global regulatory strategy for drug development programs, managing regulatory submissions across all stages of development, and ensuring compliance with international health authorities. The Director will collaborate with cross-functional teams to identify regulatory risks, guide clinical development, and shape the future of regulatory science using innovative technology-driven approaches in a fast-paced TechBio environment.

Recursion North Tyneside, NE29 8EP, United Kingdom £207,500 – £280,720 pa

Remote Permanent

Manager, Global Regulatory Science CTA

This role involves leading the operational execution of Clinical Trial Applications (CTAs) globally, outside the US, with a focus on the UK regulatory landscape. Responsibilities include managing CTA submissions, ensuring regulatory compliance, coordinating with CROs, and leveraging advanced digital tools to enhance submission efficiency.

Moderna Poland

On-site Permanent

Clinical Project Manager

As a Clinical Project Manager, you will manage clinical trial packaging and distribution projects from start to finish, acting as the main point of contact for clients and coordinating cross-functional teams. You will ensure projects meet timelines, budgets, and quality standards while maintaining compliance with GMP/GDP requirements and client processes.

Yolk Recruitment Blackwood, Cymru / Wales, United Kingdom £45,000 pa

Hybrid Permanent