Latest Project Services Jobs

Medical Director, Clinical Development, Hepatology

Lead clinical development activities for hepatology assets, contributing to clinical trial design, regulatory submissions, and cross-functional strategy. Work within project teams to advance drug development from early to registrational stages, ensuring scientific rigor and patient safety. Engage with regulators, external partners, and internal stakeholders to deliver transformative medicines for liver diseases.

GSK Stevenage, United Kingdom

Medical Director, Clinical Development, Hepatology

Lead clinical development activities for hepatology-focused drug programs, contributing to clinical trial design, regulatory submissions, and cross-functional strategy. Provide medical oversight and scientific leadership within project teams, ensuring patient safety and regulatory compliance. Engage with regulators, payors, and external experts to advance GSK’s pipeline in liver diseases.

GSK London, United Kingdom

Director, Regional Ecosystem Lead (Northern Europe & UK)

Leads CSL's engagement in the Northern Europe and UK biotech innovation ecosystems, building strategic relationships with academia, biotech firms, and investors to identify and drive partnership opportunities. Acts as a senior deal team member, sources external innovation aligned with therapeutic area priorities, and represents CSL at industry events and boards. Requires deep regional network expertise and collaboration with global R&D and business development teams to strengthen the company’s innovation pipeline.

CSL

Hybrid Permanent

Director, Biostatistics

Leads statistical strategy for global clinical development in inflammation, immunology, and specialty care, providing oversight on study design, analysis, and regulatory submissions. Manages cross-functional collaboration and drives innovation in statistical methodology. Works closely with clinical, regulatory, and data teams to ensure high-quality, compliant deliverables across the drug development lifecycle.

Pfizer United Kingdom

Manager, Statistics

Leads statistical design and analysis for clinical trials and observational studies, ensuring scientific rigor and regulatory compliance. Collaborates across functions to support drug development, regulatory submissions, and evidence generation using clinical and real-world data. Contributes to methodology research and maintains best practices within Pfizer's statistics community.

Pfizer United Kingdom

Global Labelling Associate Director, Content (Cardiovascular, Renal & Metabolism)

This role involves leading the development and maintenance of global labelling strategies and core documents for pharmaceutical products in the cardiovascular, renal, and metabolism therapeutic areas. The individual will work cross-functionally to align labelling content, interpret clinical data, and ensure compliance with global regulatory standards. Key responsibilities include supporting health authority interactions, mentoring team members, and maintaining scientific accuracy across product lifecycles.

Novartis London, United Kingdom

Hybrid Permanent

Global Labelling Associate Director, Content (Cardiovascular, Renal & Metabolism)

This role involves developing and maintaining global labelling strategies and core documentation for pharmaceutical products in the cardiovascular, renal, and metabolism therapeutic areas. The individual will lead cross-functional discussions, ensure regulatory compliance, and translate clinical data into accurate, consistent labelling content for global markets. They will also support health authority interactions and contribute to risk assessment and audit readiness.

Novartis

Hybrid Permanent

Vaccines Safety Sciences Lead

Leads and manages pharmacovigilance safety sciences functions, ensuring compliance with global regulatory standards and overseeing signal detection, safety data analysis, and process optimization. Provides strategic direction for evolving PV legislation and acts as a subject matter expert in audits and inspections. Supports drug development and post-marketing safety reporting while driving data visualization and analytical improvements.

CSL

Hybrid Permanent

Senior Scientist (In vivo Pharmacology & Translational Sciences), Cambridge, MA

Lead translational strategies for oncology and immunology programs by designing in vivo pharmacology and PK/PD studies to validate AI-designed drug candidates. Bridge computational predictions with experimental validation through CRO partnerships and biomarker-driven approaches. Drive preclinical data generation to inform clinical trial design and regulatory filings.

Isomorphic Labs England

Hybrid Permanent

Research Leader (DMPK), Cambridge, MA

Lead DMPK strategy for drug discovery projects using an AI-first approach, integrating quantitative pharmacology and ADME data to guide candidate selection. Collaborate with chemistry, pharmacology, and machine learning teams to optimise molecule design and advance predictive models. Contribute to regulatory documentation and drive innovation in human PK prediction and biotransformation understanding.

Isomorphic Labs Cambridge, United Kingdom

Principal Scientist, Bioanalytical & Molecular Assays

Lead the development and validation of molecular assays including RT-qPCR, dPCR, and NGS for clinical biomarker programs across Moderna's therapeutic pipeline. Drive end-to-end assay lifecycle management, ensure regulatory compliance with GCLP standards, and collaborate with cross-functional teams to deliver high-quality genomic data. Mentor scientists and integrate advanced analytics and AI-enabled tools to accelerate discovery and translational research.

Moderna Oxford, United Kingdom

Hybrid Permanent

Principal Scientist, Bioanalytical & Molecular Assays

This role involves leading the development and validation of advanced molecular assays—including RT-qPCR, dPCR, and NGS-based methods—for clinical biomarker programs at Moderna. The scientist will drive end-to-end assay lifecycle management, ensure compliance with GCLP and regulatory standards, and collaborate across multidisciplinary teams to generate high-quality genomic data. A key focus is integrating genomics, bioinformatics, and clinical insights to support drug development and inform future pipeline strategies.

Moderna

Hybrid Permanent

Senior Computational Biologist – Early Discovery Immunology

A Senior Computational Biologist will drive target discovery in immunology and inflammatory diseases by integrating multi-omics data (phenomics, transcriptomics, genomics, proteomics) to nominate and validate novel therapeutic targets. The role involves developing computational methods, collaborating with cross-functional teams, and translating complex analyses into actionable drug discovery programs using Recursion’s AI-driven platform.

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

Hybrid Permanent

Senior Computational Biologist - Early Discovery Oncology

Drive target discovery and validation in precision oncology by integrating multimodal biological data (phenomics, transcriptomics, genomics, proteomics) to identify novel therapeutic targets. Collaborate with cross-functional teams to develop scalable computational methods and build compelling data packages that advance drug programs. Develop criteria for target nomination and support early translational strategies using AI-powered platforms.

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

Hybrid Permanent

Executive Director / Vice President, Business Development

Lead business development strategy to identify and execute strategic partnerships, in- and out-licensing deals, co-developments, and M&A opportunities in oncology and autoimmune disease. Represent Autolus at high-level meetings, build relationships across biotech, pharma, and academia, and collaborate with cross-functional teams to align BD initiatives with corporate goals. Requires deep expertise in biopharma deal-making and strong scientific-business acumen.

Autolus