Latest Research Jobs

ViiV Healthcare (GSK) Director, Clinical Pharmacology

This role involves leading clinical pharmacology strategy across HIV drug development programs, applying PK/PD, pharmacometrics, and modeling to inform study design, regulatory decisions, and development pathways. The Director will mentor project leads, collaborate with cross-functional teams, and serve as a scientific expert in model-informed drug development, contributing to breakthroughs in HIV treatment and prevention.

GSK

Hybrid Permanent

ViiV Healthcare (GSK) Senior Director, Clinical Development

As a Senior Medical Director at ViiV Healthcare, you will lead the design and delivery of early development plans for HIV treatments, ensuring clinical excellence and medical governance across Phase 1-4 studies. You will collaborate with internal and external stakeholders to design, execute, and interpret clinical studies, focusing on long-acting medicines and ensuring patient safety and data integrity.

GSK United States

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 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

Associate Engineer, GxP IT Support

This role involves providing hands-on IT support for Moderna’s GMP manufacturing operations at the Harwell site. Key responsibilities include ensuring GMP compliance, triaging IT incidents, managing infrastructure, and collaborating with various teams to maintain robust and compliant systems. The position offers exposure to modern observability and cybersecurity tools, making it a dynamic opportunity for someone who thrives in complex, regulated environments.

Moderna Oxford, United Kingdom

On-site Permanent

Associate Engineer, GxP IT Support

This role involves supporting Moderna’s manufacturing operations at the Harwell site, ensuring GMP compliance and providing Tier 1 IT support. Responsibilities include maintaining robust IT systems, triaging incidents, managing infrastructure, and collaborating with various teams to ensure smooth operations. The position offers exposure to modern cybersecurity and automation tools, making it a dynamic and challenging opportunity in the biotech industry.

Moderna

On-site Permanent

Forward Deployed Engineer

This role involves partnering with pharmaceutical and biotechnology companies to design, build, and deploy production-grade AI solutions using Owkin K. You will work hands-on with customers, translating scientific challenges into concrete software solutions and ensuring their successful integration into complex, regulated environments.

Owkin United Kingdom

Remote Permanent

Sales Director, Life Science Accounts

This role involves leading commercial engagements with biotech companies, CROs, and life sciences investors, managing the full sales cycle from prospecting to closing deals. You will work closely with cross-functional teams to tailor solutions that align with customer goals in translational research, clinical trials, and AI-driven portfolio evaluation.

Owkin New York, United States £250,000 pa

Remote 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 Medical Director

Work with usOur team are passionate in the pursuit of excellence and in pushing the boundaries of cancer therapy and Autoimmune disease to deliver life-changing treatments to patients.Whilst working at Autolus you will enjoy a flexible, diverse and dynamic working...

Autolus London, W12 7RH, United Kingdom

Hybrid Permanent

Senior Specialist I, QA Clinical

The Senior Specialist I, QA Clinical is responsible for quality oversight in clinical development, supporting cross-functional relationships and ensuring compliance with GCP/GVP regulations. Key responsibilities include developing and implementing risk-based audit plans, conducting audits, and managing quality events. The role involves working closely with clinical project teams and external stakeholders, and maintaining the quality management system.

Autolus Stevenage, United Kingdom

Hybrid Permanent Flexible

Software Engineer (Data Services), London

This role involves working in a fast-paced, interdisciplinary team to build a cutting-edge ML-based software platform for drug discovery. Responsibilities include data engineering, service-oriented architecture, and collaboration with scientists and ML researchers to accelerate scientific breakthroughs.

Isomorphic Labs London, 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

Director, Portfolio Development Process & Standards Lead

This role leads the establishment and maintenance of processes and standards across CSL's global Portfolio Development function, ensuring high-quality clinical trial planning, evaluation, and reporting. The Director will drive process improvement, SOP governance, training curriculum development, and cross-functional change initiatives within a dynamic biotech R&D environment. They will work closely with leadership and international teams to reduce complexity, improve quality and speed, and align procedural frameworks across clinical development, biomarkers, and commercial operations.

CSL

Hybrid Permanent

Associate Director, Biostatistics (2)

The Associate Director, Biostatistics, leads the statistical contribution to clinical development programs, ensuring appropriate methodologies for study design, data analysis, and regulatory submissions. They collaborate with cross-functional teams, manage outsourcing operations, and represent Biostatistics in regulatory interactions.

CSL United Kingdom

On-site Permanent