Lead the development and application of predictive computational models and agentic workflows to evaluate target biology, safety, and translatability in drug discovery. Integrate multimodal biological data and collaborate with cross-functional teams to inform go/no-go decisions. Design and execute hypothesis-driven experiments to validate mechanisms and advance robust, reproducible methods with direct patient impact.
This role involves leading medical monitoring and safety oversight for gastrointestinal (GI) oncology clinical trials, contributing to study design, data interpretation, and regulatory interactions. The Medical Director integrates physician-level expertise into clinical development, working within cross-functional teams to ensure patient safety and scientific integrity. The position plays a key role in translating clinical data into actionable insights for advancing cancer treatments with high unmet need.
This role involves leading clinical data strategy planning and execution across Translational Medicine programs, with a focus on designing fit-for-purpose data collection approaches and supporting robust decision-making. The individual will develop Data Strategy Plans, guide trial teams on data oversight, and leverage internal and external data to inform trial design—particularly in Neuroscience. The position requires deep expertise in clinical assessments, data integrity, and cross-functional collaboration in a global, fast-paced environment.
Develop and maintain R packages and Shiny applications to support clinical trial data analysis and reporting workflows. Collaborate with statisticians and programmers to build reproducible, AI-enhanced tools, with a focus on open-source practices and modernization. Support user experience improvements and drive adoption through training and documentation.
Leads clinical development for assigned assets in Internal Medicine, driving global clinical strategy, trial design, execution, and regulatory submissions. Serves as primary clinical accountability, collaborating with cross-functional teams and external stakeholders to advance drug development programs from concept through approval, with potential focus on obesity-related therapeutics.
This role leads clinical development for Internal Medicine assets within Pfizer's Research & Development division, with accountability for designing and executing global clinical development plans. The position involves leading cross-functional teams, driving regulatory submissions, and serving as a therapeutic expert in obesity and related areas. It requires collaboration with internal and external stakeholders, including regulatory authorities and advisory boards, to shape clinical strategy and ensure successful drug development.
This role involves leading clinical development in oncology with a focus on sarcoma, providing medical oversight and strategic input across study design, execution, and data interpretation. The position ensures patient safety and clinical integrity while guiding cross-functional teams and engaging with external experts. It requires deep expertise in oncology drug development and strong leadership in a matrixed global environment.
This role involves leading clinical development strategy for sarcoma within GSK's oncology portfolio, providing medical oversight across study design, execution, and data interpretation. The Senior Medical Director will guide safety evaluation, mentor clinical teams, and represent the programme in regulatory and scientific forums. Based on-site at a GSK location with future relocation to Cambridge, UK.
This role involves providing medical and scientific leadership in safety evaluation and risk management for GSK’s clinical and post-marketing assets. The Associate Medical Director will lead safety strategy, contribute to regulatory submissions, and guide cross-functional teams in pharmacovigilance activities. The position emphasizes evidence-based decision-making, global regulatory compliance, and proactive risk communication within a matrix environment.
Leads clinical operations for a key asset across its full lifecycle, setting the operational strategy and ensuring high-quality, on-time delivery of clinical studies. Works cross-functionally to align study execution with scientific and regulatory goals, driving innovation and efficiency while managing risks and stakeholder engagement. Serves as the primary accountability point for clinical operations within global governance structures.
This role involves providing medical and scientific leadership in safety evaluation and risk management for GSK's clinical and post-marketing assets. The Associate Medical Director will lead signal detection, contribute to pharmacovigilance strategy, and ensure robust safety oversight across global development programs. Working within a cross-functional matrix, the role emphasizes evidence-based decision-making, regulatory compliance, and proactive risk communication to protect patient safety.
Provides medical and scientific leadership in safety evaluation and risk management for GSK’s clinical and post-marketing assets. Key responsibilities include signal detection, safety oversight, regulatory reporting, and contributing to global pharmacovigilance strategy. Works cross-functionally to ensure patient safety and compliance with international regulations.
This role involves providing medical and scientific leadership in the safety evaluation and risk management of GSK’s clinical and post-marketing pharmaceutical assets. The Associate Medical Director will lead signal detection, benefit-risk assessment, and pharmacovigilance strategy, ensuring robust safety oversight across global development programs. Working within a cross-functional matrix, the individual will influence safety governance, contribute to regulatory submissions, and drive evidence-based decisions to protect patient safety.
This role involves designing and implementing a global framework for Medical Science Liaison (MSL) teams, ensuring alignment across regions and markets. The position focuses on governance, performance metrics, and operational execution to enhance clinical trial engagement and scientific exchange with investigators and KOLs. It requires strategic leadership, cross-functional collaboration, and a strong understanding of medical affairs in a global biopharma context.
Leads the design and implementation of a global Medical Science Liaison (MSL) framework, focusing on governance, deployment models, and performance metrics across markets. Works cross-functionally to align medical, R&D, and regional teams, ensuring consistent scientific engagement with investigators and KOLs in support of clinical trials. Focuses on operational excellence, change enablement, and strategic evolution of field medical models in respiratory and hepatology therapeutic areas.
