Future Tech Jobs
Future Tech Jobs
Lead medical writing strategy for one or more assets, primarily in Hepatology, across clinical development stages. Design and deliver high-quality clinical documents for global regulatory submissions, lead cross-functional teams, and drive process improvements using innovative technologies. This role involves shaping submission plans, mentoring teams, and influencing regulatory outcomes in a matrix environment.
Lead the medical writing strategy for one or more pharmaceutical assets, primarily in Hepatology, ensuring high-quality clinical documents for global regulatory submissions. Drive process improvements, mentor teams, and lead complex submission projects in a matrix environment. This role involves shaping document strategy, managing cross-functional collaboration, and applying regulatory expertise across the drug development lifecycle.
Leads strategic direction and AI-driven innovation for Pfizer’s Targets and Mechanisms platforms, overseeing global teams to deliver scalable digital solutions that accelerate drug discovery. Focuses on integrating advanced data technologies, omics analytics, and predictive systems to support therapeutic target identification across research units. Works closely with R&D and digital stakeholders to align technology roadmaps with scientific and clinical priorities.
Lead the strategic direction and AI-driven innovation of Pfizer’s Targets and Mechanisms platforms, delivering scalable, science-centric digital solutions to accelerate drug discovery. Oversee a global team integrating advanced data technologies, AI, and predictive analytics across research units including Oncology, Vaccines, and Inflammation & Immunology. Shape translational biomarker frameworks and target identification strategies using large-scale omics, clinical data, and competitive intelligence to de-risk development and inform clinical decisions.
Leads cross-programme scientific strategy and integration across GSK’s hematology oncology portfolio, ensuring alignment in clinical development, biomarker strategies, and innovative trial design. Acts as a senior scientific partner to Clinical Development Leads and drives data-driven decision-making using emerging technologies like AI. Operates at the portfolio level to shape disease-area strategy and support regulatory and governance engagement.
Lead scientific and strategic integration across GSK's hematology oncology portfolio, ensuring alignment of clinical development programmes, biomarker strategies, and innovative trial designs. Drive cross-asset coordination and decision-making at the disease level, leveraging deep oncology expertise and emerging technologies like AI. Engage with internal stakeholders and external experts to shape portfolio direction and regulatory strategy.
This role leads cross-programme scientific strategy and integration across GSK’s hematology oncology portfolio, ensuring alignment in disease biology, biomarker development, and clinical trial innovation. The individual will drive portfolio-level decision-making, shape clinical development approaches using emerging technologies like AI, and engage with external experts and regulatory bodies. It is a senior individual contributor position focused on strategic coherence across multiple assets rather than direct management of a single programme.
Lead clinical development for hepatology assets within GSK’s Respiratory, Immunology & Inflammation Research Unit, driving translational research and early-phase clinical trials to validate novel liver disease targets. Provide medical oversight, design clinical development plans, and collaborate cross-functionally to advance innovative therapies from discovery through development. Work in a hybrid model with significant scientific leadership and regulatory engagement responsibilities.
This role involves leading clinical development for aging-related therapies within GSK’s Respiratory, Immunology & Inflammation Research Unit. The Medical Director will design and execute clinical development plans, provide medical oversight, and integrate translational and clinical data to advance drug candidates. The position emphasizes cross-functional leadership, regulatory engagement, and innovation in trial design to deliver differentiated medicines.
Lead clinical development for cardiovascular assets within GSK's Respiratory, Immunology & Inflammation Research Unit, driving translational and clinical strategies from early to late stages. Provide medical oversight, design studies, and collaborate across functions to deliver innovative medicines addressing unmet patient needs. Work in a hybrid model with a future relocation to Cambridge.
This role involves leading clinical development for cardiovascular assets within GSK's Respiratory, Immunology & Inflammation Research Unit. The Medical Director will design and execute clinical development plans, provide medical oversight, and collaborate across functions to advance translational and clinical studies. The position emphasizes scientific leadership, regulatory engagement, and strategic input to bring innovative medicines to patients.
This role involves leading clinical development for respiratory assets within GSK’s Respiratory, Immunology & Inflammation Research Unit. The Medical Director will design and deliver clinical and translational strategies, oversee study execution, ensure patient safety, and contribute to regulatory submissions. Working cross-functionally, they will help shape development plans that align with scientific innovation and patient needs, particularly in pulmonary hypertension and related areas.
Provides scientific leadership in oncology clinical development, contributing to study design, data interpretation, and regulatory documentation within a defined clinical programme. Works closely with cross-functional teams to ensure scientific rigor and alignment with clinical strategy, while supporting the execution of clinical studies from early to late stages. Focuses on generating robust clinical insights to advance cancer therapies with high unmet need.
Lead scientific strategy for oncology clinical studies, contributing to protocol design, data interpretation, and regulatory documentation within a global matrix team. Focus on advancing cancer therapies with high unmet need through rigorous clinical development and cross-functional collaboration. Emphasis on scientific excellence, real-world impact, and innovation in patient-focused drug development.
Lead scientific strategy for oncology clinical studies, contributing to protocol design, data interpretation, and regulatory deliverables within a global pharmaceutical environment. Collaborate across functions to ensure scientific rigor and alignment with clinical development goals, while engaging with external experts and supporting regulatory submissions. The role emphasizes innovation, data-driven decision-making, and continuous improvement in clinical development processes.
