Latest Environmental Risk Assessment Scientist Jobs

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Head of RTSM (Randomization and Trial Supply Management)

This role involves leading the RTSM function in the US, partnering with clinical development, operations, quality, and external vendors to design and deliver patient-focused randomization and clinical supply solutions. Responsibilities include managing cross-functional teams, risk assessments, process improvements, and fostering collaboration across internal and external partners.

GSK United States
Hybrid Permanent
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Regional Regulatory Intelligence Manager

This role involves leading the regional regulatory intelligence strategy, ensuring alignment with global regulatory direction and Health Authority expectations. Responsibilities include identifying and translating regulatory intelligence into actionable insights, influencing regulatory outcomes, and driving cross-functional collaboration to embed intelligence into submission processes and templates.

GSK United Kingdom
Hybrid Permanent
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Director, AI Engineering--Clinical Development and Operations (CD&O)

This role involves designing and deploying production-grade AI systems to transform clinical development and operations at scale. The Director will lead the implementation of LLMs and agentic AI in regulated workflows, building reusable, automated solutions for complex clinical processes. They will bridge technical and scientific domains, driving MLOps adoption while ensuring solutions are secure, reproducible, and aligned with enterprise data governance.

Pfizer US$176,600 – US$294,300 pa
On-site Permanent
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Director, AI Engineering--Clinical Development and Operations (CD&O)

This role involves designing and deploying production-grade AI systems to transform clinical development and operations at scale. The Director will lead the implementation of LLMs and agentic AI, building reusable workflows and decision-support tools that integrate into regulated, data-rich environments. They will bridge technical and scientific domains, driving adoption of AI solutions through collaboration with cross-functional teams and embedding MLOps best practices for scalability and reproducibility.

Pfizer US$176,600 – US$294,300 pa
On-site Permanent
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Clinical Trial Supply Manager

This role involves managing the clinical trial supply chain for GSK's global R&D studies, translating protocols into operational supply strategies, and ensuring timely delivery of investigational products. The manager coordinates across depots, logistics partners, and internal teams to maintain compliance, minimise waste, and support study milestones across all phases of clinical development.

GSK €48,375 – €116,000 pa
On-site Permanent
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Clinical Trial Supply Manager

This role involves managing the end-to-end clinical supply chain for GSK's global R&D trials, translating protocols into supply strategies, and ensuring timely delivery of investigational products. The manager will lead supply planning, coordinate with depots and logistics partners, and act as the primary link between clinical teams and supply operations across Phase I–IV studies. Emphasis is placed on risk-adjusted, patient-focused planning and continuous improvement in compliance with GxP and regulatory standards.

GSK £48,375 – £116,000 pa
On-site Permanent
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Clinical Trial Supply Manager

This role involves managing the end-to-end clinical supply chain for GSK's global R&D trials, from protocol review to study close-out. The Clinical Trial Supply Manager ensures timely, compliant delivery of investigational products by translating protocols into supply strategies, managing inventory and distribution, and acting as the key link between clinical teams and supply operations across Phase I–IV studies.

GSK €48,375 – €80,625 pa
On-site Permanent
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Clinical Trial Supply Manager

This role involves managing the end-to-end clinical supply chain for global trials from protocol review to study close-out, ensuring timely delivery of investigational products while minimizing waste. The Clinical Trial Supply Manager acts as the key link between supply chain and clinical teams, developing risk-adjusted supply strategies, overseeing depot operations, and ensuring compliance with GxP and regulatory standards across Phase I–IV studies.

GSK €48,375 – €116,000 pa
On-site Permanent
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Clinical Sciences Project Manager

This role involves managing and refining processes for investigator-sponsored research studies, supporting the Global Collaborative Studies Group in evidence generation, and leading the Request for Proposal study process. The candidate will work cross-functionally with various teams to ensure timely and compliant delivery of studies and contribute to the mission of advancing HIV research and treatment.

GSK United Kingdom
On-site Permanent
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Clinical Sciences Project Manager

This role involves developing and refining processes, risk management strategies, and other activities essential to the success of the Global Collaborative Studies Group (CSG) at ViiV Healthcare. You will lead the Request for Proposal study process, manage study-related activities, and work cross-functionally with various teams to ensure timely and compliant delivery of supported studies.

GSK
On-site Permanent
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NIS P&D Project Management, Associate Director

The NIS P&D Project Management, Associate Director role involves developing and delivering Non-Interventional Studies (NIS) project plans, managing resources, and collaborating with various functional teams to ensure accurate and aligned project schedules. Key responsibilities include maintaining data quality in Planisware, forecasting costs, and managing risks.

GSK
Hybrid Permanent
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NIS P&D Project Management, Associate Director

The NIS P&D Project Management, Associate Director is responsible for developing and delivering high-quality NIS Project Plans, managing resources, and collaborating with various functional teams to ensure alignment with R&D and marketed product portfolios. The role involves maintaining accurate project schedules, forecasting costs, and ensuring data quality in Planisware.

GSK
Hybrid Permanent
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NIS P&D Project Management, Associate Director

The NIS P&D Project Management, Associate Director is responsible for developing and delivering high-quality Non-Interventional Studies (NIS) project plans, managing resources, and collaborating with various functional teams. Key responsibilities include maintaining accurate project schedules, driving cost and resource forecasts, and ensuring alignment with strategic goals.

GSK
Hybrid Permanent
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AI Strategy Director, Development Operations

The AI Strategy Director role involves driving the AI-native Development Operations strategy at GSK, focusing on identifying and deploying AI solutions to improve clinical trial outcomes. Responsibilities include prioritizing AI opportunities, evaluating vendor capabilities, and leading cross-functional teams to prototype and deploy AI-enabled workflows.

GSK United Kingdom
On-site Permanent
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AI Strategy Director, Development Operations

The AI Strategy Director role involves driving the AI-native Development Operations strategy at GSK, focusing on identifying and deploying AI solutions to accelerate clinical trials and improve patient outcomes. Key responsibilities include prioritizing AI opportunities, evaluating external vendors, and shaping deployment strategies with cross-functional teams.

GSK
On-site Permanent