Future Tech Jobs
Future Tech Jobs
Lead clinical development for vascular programmes across early and late-phase studies, shaping clinical plans and study designs to accelerate safe, meaningful medicines for vascular disease. Work cross-functionally with translational science, regulatory, safety, and commercial teams to deliver clinical development strategies and drive innovation in cardiovascular medicine.
This role involves leading oncology clinical development for lung cancer programmes, providing medical oversight across study design, execution, and data interpretation. The Senior Medical Director ensures patient safety, guides cross-functional teams, and represents the programme in regulatory and scientific forums. Based on-site with a future relocation to Cambridge, UK, the position emphasizes strategic clinical leadership within a global biopharma environment.
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.
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.
This role involves leading clinical development activities for GSK’s oncology portfolio, with a focus on genitourinary (GU) cancers. The Senior Medical Director will design and execute Phase 1-3 clinical trials, provide medical oversight, interpret clinical data, and engage with external experts and regulatory authorities. The position requires strong leadership in a matrixed environment and deep expertise in oncology drug development.
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.
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.
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.
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.
This role leads the strategic transformation of CMC regulatory submissions at GSK, focusing on next-generation approaches such as ICH M4Q implementation, automation, and Generative AI. The Senior Director will align regulatory strategy with global enterprise initiatives, working across R&D, Quality, and Technology to shape the future of regulatory dossiers. It involves high-level stakeholder engagement, change leadership, and driving innovation in a complex, global matrix environment.
Lead scientific input into oncology clinical trial design, data interpretation, and regulatory documentation within a global pharmaceutical environment. Contribute to study-level execution and strategic insights while collaborating across multidisciplinary teams. Focus on advancing cancer therapies with high unmet need through rigorous clinical science and cross-functional partnership.
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 launch. Responsible for shaping clinical strategy, overseeing global trials, engaging with regulatory authorities, and integrating translational research and innovative approaches like AI/ML and real-world evidence. Acts as senior clinical representative in governance forums and external scientific engagements.
Leads cross-programme scientific strategy and integration across GSK’s oncology portfolio, with a focus on hematology. Provides expert guidance on disease biology, biomarker strategies, and clinical development innovation across multiple assets. Champions data-driven decision-making, trial innovation, and external engagement to align portfolio direction and accelerate development.
This role leads the strategic transformation of CMC regulatory submissions at GSK, shaping the future of dossier development through innovation in automation, Generative AI, and structured data. The Senior Director will drive alignment across regulatory, quality, manufacturing, and technology functions, championing initiatives like ICH M4Q and Project Sonata. It involves influencing senior governance, leading change, and building next-generation regulatory processes in a global, science-driven environment.
Leads the strategic transformation of CMC regulatory submissions at GSK, driving innovation through automation, Generative AI, and structured data. Works cross-functionally to align regulatory strategy with development and enterprise initiatives, including ICH M4Q and Project Sonata. Focuses on modernising the 'CMC dossier of tomorrow' within a global matrix environment.
