Lead clinical pharmacology modeling and simulation efforts for infectious disease assets, combining hands-on pharmacometric analysis with strategic input across clinical development. Design and interpret studies, develop population PK/PD models, and guide dose selection and regulatory strategies. Work within cross-functional teams to influence development decisions and advance model-informed drug development.
Lead clinical pharmacology and modelling & simulation efforts for infectious disease assets, applying pharmacokinetic/pharmacodynamic and population modelling to inform dose selection, trial design, and regulatory strategy. This senior individual contributor role combines hands-on quantitative analysis with strategic leadership across development phases, from early planning to lifecycle management. Work within a science-driven team to advance model-informed drug development using tools like NONMEM, R, and PBPK, while collaborating with cross-functional partners and supporting regulatory submissions.
The role involves leading the development and execution of precision medicine strategies within global clinical programs, focusing on biomarker and diagnostic initiatives for patient selection and regulatory support. It requires close collaboration with cross-functional teams and external partners, ensuring compliance with medical device regulations and high-quality scientific delivery. The position is embedded in the Neuroscience disease area, emphasizing strategic input into clinical trial design and regulatory submissions.
The Precision Medicine Director leads the development and execution of biomarker and diagnostic strategies within global clinical programs, focusing on patient selection and regulatory-aligned trial design. This role acts as a scientific expert, guiding cross-functional teams in neuroscience-focused initiatives and ensuring compliance with medical device regulations. The position emphasizes strategic leadership in precision medicine, with strong collaboration across clinical development, diagnostics, and external research partners.
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 for Internal Medicine assets within Pfizer's Research & Development division, with accountability for designing, executing, and interpreting global clinical studies to support regulatory submissions. The individual will act as a key clinical leader, collaborating with cross-functional teams and external stakeholders to shape clinical development plans, trial design, and lifecycle strategies. Expertise in obesity, endocrinology, or chronic weight management is required, along with leadership in managing large-scale clinical programs and regulatory deliverables.
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.
Lead government affairs and advocacy strategy across Europe and international markets, focusing on shaping policy, building relationships with EU and national stakeholders, and advancing access to HIV treatments. Develop cross-market campaigns to prioritize HIV in healthcare agendas and support uptake of long-acting innovations. Collaborate with internal teams and external partners to influence policy and drive equitable access.
