Latest Drug Discovery Jobs

Medical Director, Clinical Development (Oncology), Cambridge, MA

Leads clinical development strategy for oncology programs, translating AI-driven insights into actionable trial designs and serving as medical monitor. Collaborates with cross-functional teams to advance drug candidates from discovery through proof-of-concept, with responsibility for regulatory submissions and engagement with health authorities and key opinion leaders.

Isomorphic Labs England

Hybrid Permanent

Clinical Development Medical Director- Hepatology

Lead clinical development for hepatology assets, designing and executing translational and clinical studies to advance novel liver disease treatments. Provide medical oversight, shape development strategies, and collaborate across functions to deliver innovative medicines. Engage with regulators and external experts to drive proof-of-concept and lifecycle expansion opportunities.

GSK Stevenage, United Kingdom US$202,500 – US$371,250 pa

Hybrid Permanent

Clinical Development Senior Medical Director - Vascular

Leads clinical development for vascular programmes across early and late phases, shaping study designs and clinical development plans. Works cross-functionally with translational science, regulatory, and commercial teams to advance medicines for vascular disease, with a focus on patient impact and scientific innovation. Provides medical oversight, contributes to regulatory submissions, and guides decision-making in a matrix environment.

GSK Stevenage, United Kingdom

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, serving as the primary clinical accountability point on the Global Medicine Team. The leader designs and executes global clinical development plans, guides cross-functional teams through trial phases, and supports regulatory submissions and lifecycle strategies. Emphasis is placed on innovation, patient engagement, and strategic external collaboration to advance obesity and internal medicine therapeutics.

Pfizer

On-site Permanent

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

This role involves leading clinical development for Internal Medicine assets within Pfizer's Research & Development division, with end-to-end accountability for creating and executing global clinical development plans. The position requires deep therapeutic expertise in chronic weight management or endocrinology, leadership of cross-functional teams, and active engagement in trial design, regulatory submissions, and lifecycle strategy. The role operates in a hybrid work model and may include responsibilities across the Obesity portfolio.

Pfizer United States £274,500 – £457,500 pa

On-site 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

Associate Director, CMC Regulatory Science, International

Lead the development and execution of CMC regulatory strategies for mRNA-based products across global submissions, including IND/CTA/BLA/MAA filings. Provide expert guidance on regulatory compliance, interact with health authorities, and support quality and manufacturing teams through change controls and submissions. Work within a multidisciplinary team at the Harwell site to advance Moderna’s pipeline in vaccines, oncology, and rare diseases.

Moderna London, United Kingdom

On-site Permanent

Global Regulatory Associate Director, Life Cycle Management

This role involves managing regulatory maintenance activities for a high-complexity pharmaceutical product portfolio, ensuring compliance and timely submissions to global health authorities. The individual will lead strategic regulatory input across cross-functional teams, respond to complex queries, and support continuous process improvements. It is a hybrid or remote position with a focus on lifecycle management of innovative medicines.

Novartis £67,900 – £126,100 pa

Hybrid Permanent

Associate Director, CMC Regulatory Science, International

This role involves leading CMC regulatory strategy for global mRNA product development, preparing and reviewing regulatory submissions, and guiding cross-functional teams on compliance and agency interactions. The position requires deep expertise in biologics CMC regulations, particularly in EU and ROW markets, and plays a key part in shaping regulatory pathways across vaccines, oncology, and rare diseases. Based at the Harwell site, it emphasizes in-office collaboration within a multidisciplinary team.

Moderna

On-site Permanent

Senior Automation Engineer, Laboratory Automation & Biobanking

This role involves designing and optimizing automated laboratory workflows for biomarker testing and sample management using advanced liquid handling systems like Hamilton platforms. The engineer will lead integration of automation with data systems, develop data pipelines, and support AI-enhanced laboratory operations while ensuring compliance with GLP/GCLP standards. Collaboration with digital, QA, and vendor teams is key to delivering scalable, high-throughput solutions in a regulated clinical environment.

Moderna

Hybrid Permanent

(Fixed Term) Warehouse Specialist

Operate within a GMP-regulated warehouse environment at Moderna’s Harwell site, managing inbound and outbound material flows, inventory control via SAP, and supporting continuous mRNA manufacturing operations. Perform cycle counts, documentation, and logistics coordination while adhering to strict quality and safety standards. Gain exposure to digital-first and AI-enabled tools within a fast-paced, collaborative pharmaceutical setting.

Moderna

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

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.

Moderna

(Fixed-Term) Manufacturing Associate I

This role involves operating and maintaining equipment in a cGMP-regulated mRNA vaccine production environment, ensuring safe and compliant manufacturing processes. The associate will execute production operations, support quality assurance, troubleshoot technical issues, and contribute to continuous improvement initiatives. Work is conducted in a highly automated, digitally enabled facility with a focus on operational excellence and innovation in mRNA technology.

Moderna

Senior Manager, Packaging Engineering

Lead the technical development and implementation of a new labeling and secondary packaging operation at Moderna’s Harwell site, from initial design through commissioning and validation. Establish maintenance strategies, ensure GMP compliance, and drive continuous improvement using engineering excellence principles and digital tools. Build and lead a high-performing engineering team to support long-term operational success in a regulated biotech environment.

Moderna

Hybrid Permanent