Latest Research Associate Jobs

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

The Global Development Lead (GDL) is responsible for leading the clinical development of assigned assets in Internal Medicine. This involves designing, executing, and interpreting clinical studies, creating development plans, and collaborating with cross-functional teams to ensure regulatory approvals and global market access. The role also includes specialized monitoring, regulatory submissions, and engaging with external stakeholders to drive strategic insights.

Pfizer

On-site Permanent

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

The Global Development Lead (GDL) is responsible for leading the clinical development of assigned assets in Internal Medicine, working closely with cross-functional teams to design, execute, and interpret clinical studies. Key responsibilities include creating clinical development plans, regulatory submissions, and providing expert input on trial design and execution, while ensuring compliance and strategic insight generation.

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

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 mentoring regulatory professionals, partnering with directors on global strategies, and representing the Global Regulatory Affairs function in senior interactions and health authority meetings.

AstraZeneca Cambridge, United Kingdom

On-site Permanent

Senior Director, Global Product Lead, Early Oncology R&D

This role involves leading global product teams in early oncology R&D, from candidate selection through Phase III investment decisions. Responsibilities include shaping development strategies, engaging stakeholders, and ensuring ethical standards in oncology research.

AstraZeneca Cambridge, United Kingdom

On-site Permanent

Principal Data Strategy & Analytics Specialist

This role involves shaping data strategies and leading advanced analytics to support evidence generation and clinical decision-making using real-world and clinical trial data. The specialist will design analytical frameworks, drive data standardization, and collaborate with global teams to integrate complex data sources for patient impact.

Roche Welwyn Hatfield, United Kingdom

Hybrid Permanent

Senior Data Strategy & Analytics Specialist

This role involves designing and executing data strategies that integrate clinical, operational, and real-world data to support drug development. The specialist will act as a subject matter expert in data curation and analytics, working closely with scientific teams to improve data accessibility and usability. The position emphasizes the application of FAIR data principles and production-grade analytical workflows within a regulated environment.

Roche Welwyn Hatfield, United Kingdom

Hybrid Permanent

Bioinformatics Engineer, London

This role involves building and maintaining a high-fidelity biological data layer to support machine learning at Isomorphic Labs. You will develop large-scale bioinformatics pipelines, harmonize public and internal datasets, and collaborate with cross-functional teams to ensure data quality and standardization. Your work will directly accelerate drug discovery by providing robust, integrated biological data for AI-driven research.

Isomorphic Labs London, United Kingdom

Hybrid Permanent

Software Engineer (Inference Platform), London

This role involves developing and operating a high-performance inference platform to serve large-scale machine learning models for drug discovery. You'll work closely with research and applied ML teams to scale and harden AI systems, focusing on reliability, throughput, and infrastructure stability. The position requires expertise in distributed systems, Kubernetes, and cloud-native ML deployment.

Isomorphic Labs London, United Kingdom

Hybrid Permanent

Director, CMC Regulatory Affairs

Lead the development and execution of global CMC regulatory strategies for small molecule drugs in 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 evolving GMP standards. Collaborate closely with internal and external stakeholders to ensure timely delivery of regulatory deliverables and support clinical development programs.

Recursion London, W1C 2QP, United Kingdom

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 activities, ensuring regulatory compliance, coordinating with CROs, and leveraging advanced digital tools to enhance submission efficiency.

Moderna

On-site Permanent

Principal Scientist, Bioanalytical & Molecular Assays

This role involves leading the development and validation of advanced molecular assays (including RT-qPCR, dPCR, and NGS) to support clinical biomarker programs across Moderna’s therapeutic pipeline. The scientist will drive end-to-end assay lifecycle management, ensure regulatory compliance with GCLP standards, and collaborate with cross-functional teams to generate high-quality genomic data for clinical decision-making. Emphasis is placed on innovation, data integrity, and integrating emerging technologies like AI-enabled tools to accelerate translational research.

Moderna

Hybrid 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

AWS DevOps Engineer (Bioinformatics Experience)

AWS DevOps Engineer (Bioinformatics Sector)Oxford (1 day per month in office).£75-90k + Benefits.- This role cannot offer Visa Sponsorship.- To apply for this role you must have experience working in the Bioinformatics / Life Sciences / Genomics / BioTech sector.Your...

HAYS Specialist Recruitment Oxfordshire, United Kingdom £75,000 – £90,000 pa