Latest Vaccines Jobs

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 driving regulatory submissions. The Medical Director will collaborate across functions to generate clinical data, engage with external experts, and contribute to global development strategies. The position requires strong medical oversight, real-time safety monitoring, and leadership in oncology research with a focus on innovation and patient impact.

GSK

Hybrid Permanent

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 driving regulatory submissions. The Medical Director will collaborate with internal teams and external experts to advance GSK’s oncology pipeline, interpret clinical data, and support lifecycle management strategies. The position requires strong medical expertise in oncology and experience in clinical trial execution and regulatory processes.

GSK PLN 455,250 – PLN 758,750 pa

Hybrid Permanent

Manager, Oncology Regulatory Strategy

Lead regional regulatory strategy for oncology products across the Rest of World (ROW) region, aligning with global teams to ensure timely submissions, approvals, and commercially favorable labeling. Partner with project teams and health authorities to shape regulatory positions and influence the regional environment. Ensure compliance and effective implementation of regulatory standards throughout the product lifecycle.

Pfizer United Kingdom

Director, HTA, Value & Evidence (HV&E), Obesity Early Pipeline

Lead the development and execution of global health economics and outcomes research (HEOR) strategies for obesity and internal medicine products in early clinical development. Design and oversee real-world evidence studies, economic modeling, and patient-reported outcomes to support market access and reimbursement. Collaborate with cross-functional teams and external stakeholders to ensure evidence generation aligns with global payer and regulatory requirements.

Pfizer United States

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, Global Regulatory Science, CMC

This role leads global regulatory CMC strategy for mRNA-based medicines, developing and implementing regulatory plans for international submissions. The individual will guide CMC documentation, interact with health authorities, and provide strategic input across product development stages, ensuring compliance with EU and global regulations. The position plays a key part in advancing Moderna’s pipeline of transformative therapeutics across vaccines, oncology, and rare diseases.

Moderna

Hybrid Permanent

Senior Medical Director, Oncology Clinical Development - GU

Leads clinical development for oncology assets, focusing on genitourinary (GU) cancers, with responsibility for designing and executing global Phase 1-3 trials. Works cross-functionally to generate clinical evidence, engage key external experts, and support regulatory submissions and product launches. Operates in a matrix environment across strategy, medical affairs, and regulatory teams.

GSK Switzerland PLN 593,250 – PLN 988,750 pa

Hybrid Permanent

Senior Medical Director, Oncology Clinical Development - GU

This role involves leading clinical development for oncology therapeutics, specifically in genitourinary (GU) cancers, within a global matrix environment. The Senior Medical Director will design and execute Phase 1-3 clinical trials, ensure scientific integrity of study data, and engage with internal and external experts to advance GSK’s oncology portfolio. The position requires deep expertise in medical oncology, strong leadership in cross-functional teams, and active involvement in regulatory and strategic initiatives.

GSK PLN 593,250 – PLN 988,750 pa

Hybrid Permanent

Associate Director, Device Lead

Lead the technical ownership and global delivery of medical device platforms within GSK's manufacturing network, ensuring compliance with regulatory standards and driving innovation in device technology. Collaborate across R&D, supply chain, and quality functions to manage device lifecycle, technology transfer, and risk. Work with suppliers and internal teams to optimize manufacturing processes and support combination product development.

GSK United States £142,725 – £237,875 pa

Associate Director, Device Lead

Lead the technical ownership and lifecycle management of medical device platforms within GSK's global supply chain, ensuring regulatory compliance, technology transfer from R&D, and robust supply strategies. Drive innovation in drug delivery devices and combination products while collaborating across global teams on quality, manufacturing efficiency, and risk management. Serve as the primary technical interface between device suppliers and internal MSAT teams.

GSK £142,725 – £237,875 pa

Director, Compliance Product Manager

Lead the strategy and delivery of compliance, audit, assurance, and privacy technology products across GSK’s global operations. Oversee product roadmaps, coach product owners, and align technology with regulatory and business needs. Drive innovation in risk analytics and AI-ready platforms while ensuring security, compliance, and operational efficiency across enterprise systems.

GSK United Kingdom

Head, Oncology Clinical Development - ADCs

Lead the clinical development strategy for antibody-drug conjugates (ADCs) across multiple tumor types, from early-phase through registrational trials and market launch. Drive integrated clinical and translational research, represent the asset at key governance forums, and shape portfolio-level decision-making in oncology. Work across global cross-functional teams to advance innovative therapies within a matrixed biopharma environment.

GSK United States £242,250 – £403,750 pa

Head, Oncology Clinical Development - ADCs

Leads the end-to-end clinical development of an antibody-drug conjugate (ADC) oncology asset across multiple tumor types, from first-in-human through registrational trials and launch readiness. Responsible for shaping clinical strategy, overseeing global trials, engaging with regulatory authorities, and leading cross-functional teams in a matrixed environment. Involves governance leadership, scientific advisory boards, and integration of innovative approaches such as AI/ML and real-world evidence to accelerate development.

GSK US$242,250 – US$403,750 pa

Head, Oncology Clinical Development - ADCs

Leads the clinical development strategy for antibody-drug conjugates (ADCs) in oncology, spanning early- to late-phase trials across multiple tumor types. Responsible for end-to-end asset development, including regulatory approval and launch readiness, with a focus on scientific rigor, innovation in trial design, and cross-functional collaboration. Engages with global health authorities, governance bodies, and external experts to shape clinical and translational strategies.

GSK US$242,250 – US$403,750 pa

Head, Oncology Clinical Development - ADCs

Leads end-to-end clinical development of an antibody-drug conjugate (ADC) oncology asset across multiple tumor types, from first-in-human through registrational trials and market launch. Drives integrated clinical strategy, translational research, regulatory submissions, and cross-functional collaboration across global teams. Engages with governance bodies, scientific advisory boards, and external experts to shape development and competitive positioning.

GSK US$242,250 – US$403,750 pa