Future Tech Jobs
Future Tech Jobs
This role involves leading the global medical strategy for a lung cancer asset, working with cross-functional teams to translate scientific insights into practical patient impact. Responsibilities include chairing a global medical team, managing partnerships with academic centers, and ensuring scientific quality and compliance.
Lead a global team responsible for developing and managing oncology product labels, ensuring regulatory compliance and alignment with patient care and commercial goals. Drive strategic labelling governance, engage with regulatory authorities, and collaborate with cross-functional R&D teams to shape innovative, patient-focused labelling solutions.
Leads a global team responsible for developing and managing oncology product labeling strategies across the R&D lifecycle. This role ensures regulatory compliance, collaborates with cross-functional stakeholders, and shapes patient-focused labeling standards while advising senior leadership and engaging with regulatory authorities to drive innovation in labeling practices.
Lead a global team responsible for developing and managing oncology product labelling strategies across the R&D lifecycle. This role involves shaping compliant, patient-focused labels, advising senior stakeholders, and engaging with regulatory authorities to drive innovative approaches. The position requires strong leadership, regulatory expertise, and cross-functional collaboration within a hybrid working model.
This role involves leading a global labelling team for oncology products, shaping clear and compliant product labels that support patient care and regulatory success. The position requires strategic oversight of labelling development from early stages through lifecycle management, working closely with cross-functional teams and regulatory authorities to drive innovative, patient-focused solutions.
Leads a global team responsible for developing and managing oncology product labelling across the drug development lifecycle. This role shapes regulatory-compliant, patient-focused labels by collaborating with cross-functional stakeholders in R&D, Regulatory, Safety, and Commercial. It involves strategic decision-making, engagement with health authorities, and driving innovation in labelling standards to support GSK’s oncology portfolio.
This role involves planning and executing studies to generate robust health outcomes data for GSK's oncology products. The Director will collaborate with internal and external stakeholders to ensure evidence supports market positioning, reimbursement, and patient access. Key responsibilities include managing study timelines, ensuring deliverable quality, and translating customer needs into study concepts.
This role involves planning and executing real-world evidence studies to support the launch and market positioning of GSK's oncology drugs. The Director will collaborate with internal and external stakeholders to ensure the generation of high-quality, scientifically credible evidence that meets regulatory and payer requirements.
This role involves leading the generation of strategic insights to shape the global product strategy for a key oncology brand in GSK's ADC portfolio. Responsibilities include driving commercial forecasts, conducting market research, and collaborating with cross-functional teams to ensure insights are integrated into business decisions and investment planning.
This role involves leading the generation of strategic insights for a key oncology brand within GSK's ADC portfolio. Responsibilities include shaping commercial forecasts, conducting global market research, and partnering with cross-functional teams to drive business strategy and competitive intelligence.
The Director, Global Strategic Insights – Oncology role involves leading the generation of strategic insights to shape the global product strategy for a key oncology brand. Responsibilities include driving commercial forecasts, commissioning market research, and partnering with cross-functional teams to ensure insights are integrated into business decisions. The role requires a strong background in pharmaceuticals, oncology commercialization, and market research, with a focus on leveraging data to influence business strategy.
As a Senior Research Investigator, you will contribute to the pharmacology and translational biology strategy of novel large molecule therapeutics, leveraging Isomorphic Labs' cutting-edge AI drug design engine. You will design and execute pharmacology plans, lead in vivo and in vitro evaluations, and collaborate with interdisciplinary teams to advance drug discovery projects from early stages to clinical candidates.
As a Regulatory Conformance Officer, you will ensure that GSK's products meet all licensing and regulatory requirements, maintaining compliance with global market authorisations and supporting regulatory submissions. You will collaborate with multiple functions, including manufacturing, R&D, and global regulatory affairs, to deliver regulatory strategies and inspection readiness.
This role involves designing and deploying AI-powered tools and workflows for oncology research, building robust data infrastructure, and mentoring colleagues in computational methods. The Senior Scientist will work closely with wet-lab scientists, data science teams, and R&D IT to translate experimental data into scalable, reproducible systems.
As a Talent Partner at Isomorphic Labs, you will play a critical role in building world-class teams by developing and executing talent acquisition strategies. You will partner with senior leaders to attract top-tier talent, shape the company's future, foster an inclusive culture, and enhance the employer brand in the competitive AI and biotech landscape.
