Latest Cell Therapy Scientist Jobs

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

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

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

(Fixed Term) Scientist, Immunogenicity, Bioanalytical and Molecular Assays

This role involves designing and executing bioanalytical and immunogenicity strategies to support mRNA-based clinical development programmes. The scientist will lead assay development—including ADA, nAb, PK, and PD assays—using platforms like ELISA, MSD, and cell culture, while ensuring regulatory compliance and contributing to Moderna's expanding capabilities in Harwell. The position emphasizes collaboration across multidisciplinary teams and integration of digital and AI-enabled tools to enhance data interpretation and decision-making.

Moderna

On-site

Member of Technical Staff, Applied AI

This role involves deploying and adapting proprietary generative AI models within pharmaceutical and biotech customer environments. You'll work closely with interdisciplinary teams to integrate models into production systems, optimize performance, and translate scientific requirements into technical solutions. The position requires deep expertise in generative modelling, strong ML engineering skills, and the ability to act as a technical liaison between research and customer teams.

Latent Labs London, United Kingdom, United Kingdom

Hybrid Permanent

Forward Deployed AI Engineer

This role involves deploying and integrating generative AI models into pharmaceutical and biotech customers' scientific workflows. The engineer will lead end-to-end technical deployments, build production-grade API integrations and data pipelines, and act as a technical liaison between customers and internal research teams. A strong background in ML infrastructure, cloud platforms, and customer-facing delivery in life sciences is essential.

Latent Labs London, United Kingdom, United Kingdom

Hybrid Permanent

Vaccines Safety Sciences Lead

Leads vaccine safety sciences functions, ensuring compliance with pharmacovigilance regulations and global safety standards. Oversees signal detection, safety data analysis, and regulatory documentation while guiding process improvements and cross-functional initiatives. Manages teams and supports regulatory inspections, safety reporting, and the implementation of data visualization tools for enhanced decision-making.

CSL

Hybrid Permanent

Associate Director, Biostatistics

This role leads the statistical strategy for clinical development programs, overseeing study design, data analysis, and regulatory submissions. The individual will guide biostatistical input across trials, interact with regulatory authorities, and ensure accurate reporting of results. Collaboration with cross-functional teams and oversight of internal or outsourced programming efforts are key aspects of the position.

CSL

Hybrid Permanent

Global Safety Lead - Formulation Safety

Leads global safety strategy for formulation safety across the product lifecycle, focusing on clinical safety evaluation, signal detection, and risk management. Oversees production of key pharmacovigilance documents and ensures compliance with regulatory standards. Acts as safety representative in cross-functional teams and drives safety specifications and risk mitigation plans.

CSL

Global Safety Lead - Formulation Safety

Leads global safety strategy for formulation safety within CSL's GSPV department, overseeing clinical safety evaluation across product lifecycles. Responsible for signal detection, risk management planning, and regulatory compliance across clinical development and post-marketing phases. Serves as safety representative in cross-functional teams, ensuring alignment with medical, regulatory, and business objectives.

CSL

Associate Director, Clinical Trial Disclosure & Transparency

This role leads global clinical trial disclosure and transparency strategy, ensuring compliance with international regulations such as FDAAA 801, EU CTR, and MHRA requirements. The individual oversees study registration, results reporting, and layperson summaries, while managing redaction of confidential information for public release. They act as a key liaison with regulatory bodies and internal teams, driving process efficiency and vendor performance across the clinical development lifecycle.

CSL

Senior Director, Search & Evaluation Late TA Lead, Immunology

This role involves leading strategic sourcing and evaluation of late-stage external Hematology therapeutic assets, engaging with key opinion leaders, and integrating innovation into portfolio planning. The position requires deep clinical expertise, a proven track record in deal-making, and strong collaboration with cross-functional teams.

CSL US$263,000 – US$328,000 pa

Hybrid Permanent

Senior Director, Search & Evaluation Late TA Lead, Immunology

Lead the strategic sourcing and evaluation of late-stage therapeutic assets in Immunology, Hematology, or related areas, from Phase 2 through marketed drugs. Drive cross-functional due diligence, engage with key opinion leaders and clinical networks, and shape portfolio strategy through high-impact partnerships and transactions. Operate within a global biotech ecosystem with strong collaboration across R&D, BD, and regulatory functions.

CSL US$263,000 – US$328,000 pa

Hybrid Permanent

Case Management Intake Manager

Oversees the vendor responsible for logging and triaging global adverse event reports in CSL's pharmacovigilance system, ensuring accurate, timely, and compliant case intake. Develops guidance, provides training, and maintains audit readiness for regulatory compliance. Acts as subject matter expert on intake processes across cross-functional projects and procedural documentation.

CSL United Kingdom

GLP/GCLP Vendor Oversight and QA Lead (EU)

This role focuses on end-to-end quality oversight of external vendors and suppliers involved in regulated R&D activities, ensuring compliance with GLP, GCP, GMP, and GVP standards. The individual will lead vendor qualification, audit management, quality agreement negotiation, and continuous performance monitoring, while collaborating with cross-functional teams including Clinical, CMC, Safety, and Legal. A key aspect is driving compliance, data integrity (ALCOA+), and continuous improvement across third-party partners through risk-based assessments, CAPA follow-up, and QMS integration.

CSL United Kingdom

On-site Permanent