Latest Pharmaceutical Scientist Jobs

Director, Global Real-World Evidence & Health Outcomes Research Scientist- Hepatology

Leads the design and execution of real-world evidence (RWE) and health outcomes studies to support GSK's hepatology assets, ensuring robust data generation for market access, reimbursement, and patient impact. Works cross-functionally with medical, commercial, and R&D teams to align evidence strategies with global regulatory and payer requirements. Focuses on translating complex data into actionable insights for diverse stakeholders.

GSK £185,250 – £339,625 pa

Remote Permanent

Director, Global Real-World Evidence & Health Outcomes Research Scientist- Hepatology

Lead the development and execution of real-world evidence and health outcomes research to support GSK's hepatology assets. Drive strategic evidence generation aligned with regulatory, reimbursement, and market access needs, working across global teams and external partners. Focus on robust study design, data analysis, and dissemination to influence decision-making across payers, providers, and health systems.

GSK US$185,250 – US$308,750 pa

Head of DMPK

Leads DMPK strategy to advance drug programs from discovery to clinical development, integrating predictive modeling and high-throughput data. Builds and guides a scientific team while collaborating across functions and external partners to de-risk and accelerate therapeutic pipelines with a tech-forward approach.

Recursion London, United Kingdom £166,500 – £208,100 pa

Hybrid Permanent

Head of DMPK

Leads the development and execution of DMPK strategy across drug discovery and development programs, integrating predictive ADME modeling and high-throughput experimental data. Bridges computational and experimental teams to accelerate small molecule and emerging modality programs from hit identification through IND-enabling studies. Builds and mentors a high-performing DMPK team within a cross-functional, tech-driven drug discovery environment.

Recursion United Kingdom US$284,900 – US$400,950 pa

Hybrid Permanent

Field Service Engineer, Medical Diagnostic Systems

Perform on-site service and breakdown repair of advanced medical diagnostic systems in NHS and private laboratory settings. Provide technical troubleshooting support and collaborate with lab managers and technicians. Receive full product training and work a five-day week including some weekends.

TRS Consulting Aldershot, Hampshire, GU11 1BX, United Kingdom £52,000 pa

Field Service Engineer, Medical Diagnostic Systems

Perform installation, maintenance, and repair of advanced medical diagnostic systems in NHS and private laboratories. Provide on-site technical support and troubleshooting, working closely with lab staff across diverse healthcare settings. Role includes extensive field work with full product training provided.

TRS Consulting Winchester, Hampshire, United Kingdom £52,000 pa

On-site Permanent

Senior Sales Executive - Clinical Diagnostic Testing Services

This role involves driving business development for AI-powered diagnostic testing services across the UK, targeting life sciences, pharmaceutical, and clinical research clients. The Senior Sales Executive will lead end-to-end sales cycles, build strategic relationships with scientific and commercial stakeholders, and represent the company at industry events. Success requires a consultative, self-driven approach to selling complex service solutions in a remote-working environment.

Tech Buildr Liverpool, Merseyside, United Kingdom £45,000 – £65,000 pa

Remote Permanent

Clinical Data Strategy, Manager

This role involves designing and executing data strategy plans for clinical trials within Novartis' Translational Medicine portfolio, with a focus on early data planning, risk assessment, and alignment of data collection with scientific objectives. The position supports trial design and data oversight, particularly in the Neuroscience Therapeutic Area, and ensures high-quality, consistent data to enable rapid, data-driven decision-making across global teams.

Novartis London, United Kingdom £49,140 – £91,260 pa

Hybrid Permanent

Senior Clinical Trial Case Manager

Manages clinical trial case management activities, ensuring compliance with international and national regulations including GxP and pharmacovigilance standards. Oversees safety reporting, vendor performance, and case processing for serious adverse events, while acting as a key liaison for inspections and audits. Provides training, supports database enhancements, and ensures accurate coding and consistency in safety data analysis.

CSL

Vaccines Safety Sciences Lead

Leads and manages pharmacovigilance functions, ensuring compliance with global regulatory standards and GxP guidelines. Oversees signal detection, safety data analysis, and regulatory documentation while providing strategic direction for process improvements and inspection readiness. Acts as a subject matter expert in safety sciences, leading teams and contributing to drug development and post-marketing safety initiatives.

CSL

Hybrid Permanent

Executive Regulatory Science Director, Respiratory & Immunology

This role leads global regulatory strategy for respiratory and immunology therapies across all development stages, from early research to post-marketing. The director will mentor regulatory leads, shape policy, and engage with health authorities like the FDA and EMA to secure rapid approvals with competitive labelling. They will influence key governance decisions and integrate emerging science into regulatory planning.

AstraZeneca Cambridge, United Kingdom

Associate Director, Global Regulatory Science, CMC

Leads global regulatory strategy for CMC (Chemistry, Manufacturing, and Controls) in support of mRNA-based medicines, ensuring compliance with international regulations and guiding submissions across multiple therapeutic areas. Works closely with manufacturing, quality, and development teams to prepare high-quality regulatory documentation and engage with health authorities. Focuses on biologics, particularly in vaccines, oncology, and rare diseases, within a rapidly expanding biotech environment.

Moderna London, United Kingdom

Hybrid Permanent

Associate Director, CMC Regulatory Affairs, International

This role involves leading CMC regulatory strategies for international submissions, including IND/CTA/BLA/MAA filings, with a focus on mRNA-based medicines. The individual will guide global regulatory compliance, interact with health authorities, and support quality and manufacturing teams across therapeutic areas like vaccines, oncology, and rare diseases. It requires deep expertise in biologics CMC regulations and a proactive approach to navigating complex regulatory landscapes.

Moderna London, United Kingdom

On-site Permanent

Health Economics Manager

Job Title: Health Economics ManagerLocation: Pancras Square, LondonCompetitive salary and benefitsAbout the RoleWe are seeking an experienced Health Economics Manager to lead the development and delivery of health economic strategies and evidence that demonstrate the value of innovative therapies and...

AstraZeneca London, United Kingdom

Sr. Manager, RWE/EPI Internal Medicine

This role involves leading real-world evidence and epidemiological research to support Pfizer's Internal Medicine drug development and medical strategy. The individual will design and conduct global studies, synthesize literature, and generate insights from real-world data sources, while collaborating with cross-functional teams and external partners. They will also contribute to regulatory submissions and scientific communications, ensuring high-quality, compliant research outputs.

Pfizer Cambridge, United Kingdom

Hybrid Permanent