Latest Life Sciences Jobs

Oncology Medical Head, International

This role involves defining and executing the international medical strategy for Pfizer’s Oncology portfolio, collaborating with global and regional teams to ensure patient-centered, evidence-driven medical impact. Responsibilities include leading the scientific narrative, data interpretation, and communication across regions, as well as engaging with clinical and research leaders to drive strategic decisions and continuous improvement.

Pfizer

On-site Permanent

Oncology Medical Head, International

This senior leadership role involves defining and executing the international medical strategy for Pfizer’s Oncology portfolio, collaborating with global teams to ensure patient-centered, evidence-driven medical impact. The role requires deep oncology expertise and strong leadership to drive strategic decisions and medical execution across regions.

Pfizer

On-site Permanent

Oncology Medical Head, International

This role involves defining and executing the international medical strategy for Pfizer’s Oncology portfolio, collaborating with global and regional teams to ensure patient-centered, evidence-driven decisions. The position requires deep oncology expertise and leadership to drive medical impact across international markets.

Pfizer

On-site Permanent

Oncology Medical Head, International

This senior leadership role involves defining and executing the international medical strategy for Pfizer’s Oncology portfolio, ensuring patient-centered, evidence-driven decisions and high-quality medical execution across regions. The role requires deep oncology expertise, strategic thinking, and collaboration with global and regional stakeholders to drive the oncology scientific narrative and data interpretation.

Pfizer

On-site Permanent

Oncology Medical Head, International

This senior leadership role involves defining and executing the international medical strategy for Pfizer’s Oncology portfolio, ensuring patient-centered, evidence-driven decisions, and leading interactions with clinical and research experts. The role requires deep oncology expertise and strong leadership to drive medical impact globally.

Pfizer

On-site Permanent

Global Program Regulatory Manager - Neuroscience

This role involves driving regulatory strategy and execution for neuroscience products across global markets, with a focus on preparing high-quality submissions and managing interactions with health authorities. The manager will coordinate clinical trial applications, support approvals, and ensure compliance throughout the product lifecycle. Collaboration with cross-functional teams is essential to translate scientific data into regulatory outcomes.

Novartis London, United Kingdom

Hybrid Permanent

Global Program Regulatory Manager - Neuroscience

This role involves driving regulatory strategy and execution for neuroscience products across global markets, with a focus on preparing and submitting clinical trial applications, managing health authority interactions, and ensuring compliance throughout the product lifecycle. The manager will work cross-functionally to translate scientific data into regulatory submissions and support timely approvals. It is a hybrid role based in London, requiring strong expertise in pharmaceutical regulatory affairs.

Novartis

Hybrid Permanent

Clinical Development Medical Director - Neuromuscular

This role involves providing clinical leadership in neuroscience drug development, with a focus on neuromuscular or related neurological disorders. The Medical Director will shape global clinical strategy, lead trial execution, and guide regulatory submissions while collaborating with cross-functional teams and external experts. It emphasizes scientific innovation, particularly in gene therapy, within a dynamic, international environment.

Novartis Ireland €90,300 – €167,700 pa

Hybrid Permanent

Medical Director, Gastroenterology, Early Clinical Development

This role involves leading global clinical trial teams through phase 1 and 2 development, drafting early clinical development plans, and serving as a medical lead for early clinical studies. The Medical Director will collaborate with biomarker experts, research scientists, and key opinion leaders to identify and implement strategies for preclinical and clinical support of gastroenterology programs.

Novartis London, United Kingdom

Hybrid Permanent

Vendor Start-Up Manager - eCOA & Translations

The Vendor Start-Up Manager for eCOA and Translations ensures vendors are aligned and ready to deliver high-quality services from protocol finalization to database go-live. Key responsibilities include reviewing vendor specifications, coordinating kick-off meetings, performing User Acceptance Testing, and optimizing the study start-up process.

Novartis London, United Kingdom

Hybrid Permanent

Vendor Start-Up Manager - eCOA & Translations

The Vendor Start-Up Manager for eCOA and Translations ensures vendors are aligned and ready to deliver, protecting study timelines, quality, and patient experience. Key responsibilities include technical expertise, risk assessment, continuous improvement, and vendor oversight.

Novartis

Hybrid Permanent

Global Regulatory Associate Director, Life Cycle Management

This role involves managing regulatory maintenance for a high-complexity pharmaceutical portfolio, ensuring compliance and timely submissions to global health authorities. The candidate will lead strategic regulatory input across cross-functional teams, respond to complex queries, and support continuous improvement initiatives. It's a key position influencing patient access to medicines through robust lifecycle management.

Novartis London, United Kingdom £67,900 – £126,100 pa

Hybrid Permanent

Associate Director, Regulatory Diagnostics

Designs and leads global regulatory strategies for precision diagnostics, including companion diagnostics and in vitro devices, integrated within drug development programs. Works cross-functionally to manage submissions, health authority interactions, and compliance across lifecycle stages in a collaborative, innovation-driven environment.

Novartis London, United Kingdom £67,900 – £126,100 pa

Hybrid Permanent

Trial Master File Oversight Manager

This role involves overseeing the quality and completeness of Trial Master Files across global clinical trials, ensuring compliance and readiness for audits. The manager will lead vendor oversight, identify documentation risks, and drive process improvements while acting as a subject matter expert. Collaboration with cross-functional teams is essential to maintain high standards in clinical documentation and support continuous innovation in TMF systems.

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

Hybrid Permanent

Global Regulatory Associate Director, Life Cycle Management

Manages regulatory maintenance for a high-complexity pharmaceutical portfolio, ensuring compliance and timely submissions to global health authorities. Develops strategic input on safety reports, variations, and renewals, while leading responses to regulatory queries and supporting cross-functional initiatives. Plays a key role in lifecycle management of innovative medicines, requiring strong scientific interpretation and stakeholder collaboration.

Novartis £67,900 – £126,100 pa

Hybrid Permanent