Latest Pharmaceuticals Jobs

Associate Director, Regulatory Affairs

This role involves leading the development of global regulatory strategies for drug development programs, managing regulatory activities, and collaborating with cross-functional teams. The position requires extensive experience in regulatory affairs, with a focus on global health authorities and regulatory submissions.

Recursion North Tyneside, NE29 8EP, United Kingdom

On-site Permanent

Vice President, Head of Clinical Operations

This role involves leading the clinical operations strategy and execution across Recursion’s full clinical portfolio, from early-stage studies to pivotal trials and submission support. The VP will build scalable operating models, manage global trials, and ensure operational excellence in a data-driven, patient-centered, and technology-enabled environment.

Recursion North Tyneside, NE29 8EP, United Kingdom

On-site Permanent

Senior Director, Global Health Outcomes, ViiV Healthcare

This role involves leading the global health outcomes function at ViiV Healthcare, designing and delivering robust evidence to support HIV treatment and prevention medicines. Responsibilities include strategic leadership, evidence generation, and collaboration with various stakeholders to optimize patient access and value demonstration.

GSK

On-site Permanent

Senior Director, Head of Global Medical Governance, ViiV Healthcare

This role involves leading the global medical governance system at ViiV Healthcare, ensuring compliance and ethical standards across all medical activities. Responsibilities include developing and maintaining governance policies, advocating for medical governance, and collaborating with regional teams to embed best practices.

GSK United Kingdom

On-site Permanent

Head of Make CoE

The Head of Make CoE will lead the transformation of end-to-end manufacturing processes across a global network, partnering with sites and central teams to deliver safer, higher-quality, more sustainable, and more productive operations. Key responsibilities include strategy and roadmap leadership, governance, cross-functional integration, and team development, with a focus on digital and autonomous manufacturing.

AstraZeneca Macclesfield, United Kingdom

Hybrid Permanent

Feasibility and Recruitment Lead

This role involves leading UK feasibility and recruitment for cutting-edge cell therapy studies, translating scientific insights into actionable plans. Responsibilities include guiding end-to-end feasibility, collaborating with global stakeholders, and developing recruitment strategies to ensure timely and effective patient access to trials.

AstraZeneca Cambridge, United Kingdom

On-site Permanent

(Fixed-Term) Manufacturing Associate, Drug Substance - Shift Position

The Role:Joining Moderna offers the unique opportunity to be part of a pioneering team that's revolutionizing medicine through mRNA technology, with a diverse pipeline of development programs across various diseases.As an employee, you'll be part of a continually growing organization,...

Moderna Oxford, United Kingdom

(Fixed-Term) Manufacturing Associate II - Shift Position

The Role:Joining Moderna offers the unique opportunity to be part of a pioneering team that's revolutionizing medicine through mRNA technology with a diverse pipeline of development programs across various diseases.As an employee, you'll be part of a continually growing organization...

Moderna Oxford, United Kingdom

GCP Compliance Manager - Clinical Programs & Trials

This role involves providing compliance oversight for clinical programs and trials, ensuring adherence to Good Clinical Practice standards. You will act as a primary compliance partner to Clinical Trial Teams, enabling decision-making on complex regulatory scenarios and leading cross-functional discussions to resolve quality issues.

Novartis Ireland

Hybrid Permanent

Senior Scientific Engagement & Program Manager

This role involves planning and executing high-quality medical and scientific engagement activities across various therapeutic areas, including Oncology, Cardiovascular Disease, and Immunology. The Senior Scientific Engagement & Program Manager will coordinate advisory boards, congress activities, and medical education programs, ensuring seamless delivery and continuous improvement in processes and tools.

Novartis London, United Kingdom

Hybrid Permanent

DMPK Lead, London

As a DMPK Lead, you will drive the DMPK strategy for drug discovery projects, integrating quantitative pharmacology and AI-first approaches. You will design and implement DMPK strategies, optimize the use of datasets, and collaborate with interdisciplinary teams to advance drug design and development.

Isomorphic Labs United Kingdom

Hybrid 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

ML Research Engineer, London

This role involves translating research concepts into practical AI implementations, optimizing models, and collaborating with scientists and engineers to advance drug discovery. You will work on state-of-the-art ML models, design experiments, and develop specialized tools to support the team's innovative projects.

Isomorphic Labs London, United Kingdom

On-site Permanent

Quality Oversight and Compliance Director

The Quality Oversight and Compliance Director at Pfizer is responsible for developing and maintaining quality plans, ensuring inspection and audit readiness, and providing quality oversight of process deviations and investigations. This role involves interpreting and applying global regulations, driving compliance, and collaborating with stakeholders to identify and mitigate risks, ensuring the quality and integrity of Pfizer's medicines and vaccines.

Pfizer Sandwich, United Kingdom

On-site Permanent