Latest Pharmaceuticals Jobs

Director, Clinical Science

Lead and oversee clinical aspects of early-phase drug trials, including protocol development, medical monitoring, data review, and site engagement. Collaborate cross-functionally to ensure data integrity and trial execution across multiple oncology and hematology projects. Present findings internally and externally, and contribute to IND-enabling studies within an AI-driven drug discovery environment.

Recursion United Kingdom US$212,900 – US$287,980 pa

Remote Permanent

Senior Computational Biologist – Early Discovery Immunology

A Senior Computational Biologist will lead target discovery and validation in immunology and inflammatory diseases by integrating multimodal biological data from Recursion’s platform. The role involves developing computational methods, collaborating across disciplines, and driving data-informed decisions to advance drug programs. The scientist will work closely with biologists, chemists, and engineers in a fast-paced, AI-driven environment focused on accelerating therapeutic development.

Recursion United Kingdom £151,800 – £220,660 pa

Hybrid Permanent

Audit Senior Lead (EMEA GMP Audit)

This role involves performing and managing GMP and compliance audits of GSK's Biopharm, Vaccines, and Pharmaceutical facilities across the EMEA region. You will evaluate compliance with GMP, regulatory requirements, and quality management systems, and provide subject matter expertise in sterile manufacturing. The role requires strong communication and influencing skills to engage with senior stakeholders and produce clear audit reports.

GSK Worthing, United Kingdom

Hybrid Permanent

Audit Senior Lead (EMEA GMP Audit)

The Audit Senior Lead role involves performing and managing GMP and compliance audits of GSK's Biopharm, Vaccines, and Pharmaceutical facilities. Responsibilities include evaluating compliance, conducting various types of audits, and producing clear audit reports to inform senior management of risks and corrective actions.

GSK Barnard Castle, United Kingdom

Hybrid Permanent

Director, Sustainability

This role leads sustainability strategy within AstraZeneca's Chemical Development department, embedding green chemistry principles across process development and commercialisation. The director will drive innovation in environmental sustainability, oversee compliance, and act as a key advisor to CDMO partners to reduce carbon footprint and resource consumption across the supply chain. Collaboration with cross-functional teams and external stakeholders is central to advancing the company’s long-term sustainability goals.

AstraZeneca Macclesfield, United Kingdom

Hybrid Permanent

Director, Clinical Intelligence & Evidence – Cardiovascular, Renal and Metabolism

Role: Director, Clinical Intelligence & Evidence – Cardiovascular, Renal and MetabolismLocation: Cambridge UKSalary: Competitive + Excellent BenefitsAt AstraZeneca make a meaningful impact that brings real benefits to society. By applying your knowledge of data, you will help to redefine our...

AstraZeneca Cambridge, United Kingdom

Director Biostatistics - Hematology

The Director of Biostatistics leads the statistical aspects of clinical development programs, ensuring robust study design, data analysis, and regulatory submissions. They collaborate closely with cross-functional teams and regulatory authorities to drive the success of clinical trials and ensure high-quality statistical insights.

CSL

Hybrid Permanent

Associate Director, Medical Affairs

This role involves shaping medical strategy for immunology products, supporting post-launch lifecycle management, and driving scientific engagement with key opinion leaders and patient groups. The individual will coordinate investigator-led studies, provide scientific input to commercial teams, and support evidence generation across global markets. Collaboration with cross-functional teams and affiliates is central to advancing clinical understanding and therapeutic impact.

CSL United Kingdom

Hybrid Permanent

Associate Director, CMC Regulatory Science, International

This role involves developing and implementing CMC regulatory strategies for global submissions, providing guidance on regulatory CMC aspects, and ensuring compliance with health authority guidelines. The candidate will support multiple programs in various therapeutic areas, including vaccines, oncology, and rare diseases, and contribute to the development of regulatory processes and procedures.

Moderna

On-site 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

Translational Medicine Expert – Dermatology, Associate Director

This role involves leading translational medicine strategies in dermatology, spanning early to late-stage drug development. The expert will drive clinical pharmacology, biomarker development, and regulatory strategies while collaborating across research, development, and external stakeholders. Key responsibilities include study design, safety oversight, and scientific leadership in global project teams.

Novartis London, United Kingdom £67,900 – £126,100 pa

Hybrid Permanent

Director, Development Unit CQA Program Lead

Salary Range:£78,400.00 - £145,600.00Job Description Summary#LI-HybridLocation: London (The Westworks), United KingdomRelocation Support: This role is based in London (The Westworks), United Kingdom. Novartis is unable to offer relocation support: please only apply if accessible.Shaping the future of clinical development requires...

Novartis London, United Kingdom

Cluster HTA Hub Senior Manager

In this role, you will develop and lead complex projects, manage economic research studies for clinical trials, and formulate research plans. You will also collaborate with sales teams to maximize sales and enhance customer interactions using health economic models.

Pfizer London, N1 5EA, United Kingdom

Hybrid Permanent

Director, Clinical Trial and Data Transparency

This role involves providing strategic and operational expertise for the disclosure of clinical regulatory documents on public websites, ensuring compliance with global regulatory requirements. Responsibilities include managing disclosure activities, overseeing vendors, and developing standard processes and technologic solutions to support transparency in clinical trials.

Pfizer India

Remote Permanent

PKPD Modelling Lead, London

Isomorphic Labs is applying frontier AI to help unlock deeper scientific insights, faster breakthroughs, and life-changing medicines with an ambition to solve all disease.The future is coming. A future enabled and enriched by the incredible power of machine learning. A...

Isomorphic Labs London, United Kingdom