Latest Healthcare Jobs

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Executive Medical Director, Clinical Development Lead - Oncology

Leads clinical development strategy for oncology assets, defining scientific narrative, benefit-risk frameworks, and decision-making across the asset lifecycle. Serves as the primary clinical authority, guiding governance, regulatory engagement, and cross-functional alignment while leveraging AI and advanced analytics to accelerate development. Mentors clinical talent and shapes enterprise-level standards in a dynamic R&D environment.

GSK US$242,250 – US$403,750 pa
Hybrid Permanent
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Executive Medical Director, Clinical Development Lead - Oncology

Leads clinical development strategy for oncology assets, defining scientific narratives and benefit-risk frameworks across the product lifecycle. Serves as the primary clinical authority, guiding governance decisions and representing Clinical Development in internal and external forums. Integrates AI-driven insights and advanced analytics to accelerate data-informed decision-making and shape innovative development pathways in cancer therapeutics.

GSK US$242,250 – US$403,750 pa
Hybrid Permanent
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Director, Resilience Lifecycle & Supply Chain Operations

Leads end-to-end product lifecycle management and supply chain operations across the UK, Canada, and Australia, aligning global strategies with local execution. Focuses on launch planning, supply chain resilience, cross-market coordination, and operational governance. Drives standardization, crisis preparedness, and continuous improvement through cross-functional leadership and digital transformation initiatives.

Moderna United States US$167,000 – US$300,700 pa
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Director, Resilience Lifecycle & Supply Chain Operations

Leads end-to-end product lifecycle management, launch planning, and supply chain operations across the UK, Canada, and Australia, ensuring alignment between global strategy and local execution. Establishes governance, performance standards, and escalation frameworks while driving operational resilience, compliance, and cross-market collaboration. Focuses on S&OP, business continuity, crisis preparedness, and digital transformation through analytics and automation.

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Global Development Lead, Internal Medicine, Sr. Director (non-MD)

This role involves leading clinical development for internal medicine assets within Pfizer's Research & Development division, with a focus on obesity-related therapeutics. The Global Development Lead serves as the primary clinical accountability point, designing and executing global clinical development plans, regulatory submissions, and cross-functional team leadership. The position requires deep expertise in endocrinology or chronic weight management and extensive experience in Phase 1-3 clinical trials, translational medicine, and regulatory strategy across global markets.

Pfizer United States £214,900 – £358,100 pa
On-site Permanent
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Global Development Lead, Internal Medicine, Sr. Director (non-MD)

This role leads clinical development for assigned assets in Internal Medicine within Pfizer's R&D division, with accountability for designing and executing global clinical development plans. The individual will guide cross-functional teams through trial design, regulatory submissions, and lifecycle management, while serving as a therapeutic expert and strategic partner across internal and external stakeholders. Emphasis is placed on innovation, patient engagement, and compliance with global regulatory standards.

Pfizer £214,900 – £358,100 pa
On-site Permanent
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Associate Director of Clinical Sciences

This role involves leading clinical sciences activities within global oncology R&D, focusing on study design, protocol development, and clinical data review across the development lifecycle. The individual will act as a subject matter expert, ensuring scientific rigor and regulatory compliance while collaborating with cross-functional teams and external partners. A key focus is on immuno-oncology, with responsibilities spanning from early-phase to late-stage clinical development.

GSK
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Clinical Operations Specialist (Finance)

The role involves managing financial aspects of clinical trials in the UK, including budget tracking, forecasting, and ensuring timely payments to investigator sites and vendors in compliance with regulations. The specialist supports the local delivery lead, coordinates with global and local teams, and leverages AI and digital tools to improve clinical trial efficiency. Administrative duties include meeting coordination, communication management, and maintaining compliance with SOPs and audit requirements.

GSK United Kingdom
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Product Director, Evidence Preparation

Lead the strategy and development of AI-enabled digital products for structured authoring of regulatory and clinical evidence content across GSK’s R&D function. Drive innovation in modular content management, automation, and AI-assisted workflows while ensuring compliance with GxP and data integrity standards. Collaborate with cross-functional scientific and technical teams to scale enterprise-grade solutions.

GSK United Kingdom
Hybrid Permanent
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Senior Medical Director, Oncology Clinical Development - GU

Lead clinical development for oncology assets, focusing on genitourinary (GU) cancers, with responsibility for designing and executing global Phase 1-3 trials. Drive medical strategy, collaborate with key external experts, and ensure scientific integrity across clinical programs. Work within a matrix environment to support regulatory filings and lifecycle management of innovative therapies.

GSK £284,250 – £473,750 pa
Hybrid Permanent
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Senior Medical Director, Oncology Clinical Development - GU

This role involves leading clinical development for oncology assets, specifically in genitourinary (GU) cancers, within a global matrix environment. The Senior Medical Director will design and execute phase 1–3 clinical trials, provide medical oversight, interpret study data, and engage with external experts and regulatory authorities. The position plays a key strategic role in advancing GSK’s oncology pipeline from development through regulatory approval and lifecycle management.

GSK US$284,250 – US$473,750 pa
On-site Permanent
GSK logo

Senior Medical Director, Oncology Clinical Development - GU

Leads clinical development of oncology assets, focusing on genitourinary (GU) cancers, with responsibility for designing and executing global Phase 1-3 trials. Provides medical oversight, interprets clinical data, and collaborates with regulatory teams and external experts. Works within a matrixed environment to advance GSK’s oncology pipeline from development through regulatory approval and market launch.

GSK PLN 593,250 – PLN 988,750 pa
Hybrid Permanent
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Medical Director, Oncology Clinical Development

This role involves leading clinical development activities for oncology assets, including designing and executing phase 1-3 trials, ensuring scientific integrity, and generating clinical data to support regulatory approvals. The Medical Director will collaborate with cross-functional teams and external experts to advance GSK’s oncology pipeline, with a focus on innovative therapies. The position requires strong medical expertise in oncology and experience in clinical trial management and regulatory processes.

GSK US$222,750 – US$371,250 pa
Hybrid Permanent
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Senior Research Associate, Bioanalytical & Molecular Assays

This role involves developing, optimizing, and validating molecular bioanalytical assays—such as qPCR, ddPCR, and RNA isolation—to support mRNA-based clinical programs. The scientist will work within GCL0-compliant (GCLP) frameworks to generate pharmacokinetic and pharmacodynamic data, ensuring regulatory compliance and data integrity. Collaboration with cross-functional teams and adoption of digital tools and automation are key to advancing clinical trial execution and analytical processes.

Hybrid Permanent
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Principal Scientist, Immunogenicity and Ligand Binding Assays

This role involves leading scientific strategy and execution for immunogenicity and ligand binding assays (LBA) in support of Moderna’s mRNA-LNP therapeutic programs. The Principal Scientist will oversee regulated bioanalytical activities including assay development, validation, and sample analysis, ensuring compliance with GcLP, GLP, and GCP standards. The position plays a key role in clinical development by generating high-quality data to inform regulatory submissions and advance innovative medicines, with opportunities to engage in AI-enabled and digital analytical approaches.

Hybrid Permanent