This role involves leading clinical development for aging-related research within GSK’s Respiratory, Immunology & Inflammation 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 addressing unmet needs in aging and immune science.
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.
This role involves leading clinical development for Internal Medicine assets within Pfizer's Research & Development division, with a focus on obesity-related therapies. The Global Development Lead serves as the primary clinical accountability point, designing and executing global clinical development plans, regulatory submissions, and cross-functional team leadership. The position requires deep therapeutic expertise in endocrinology or internal medicine, extensive experience in Phase 1–3 trials, and strategic input into product development, digital innovation, and patient engagement initiatives.
This role involves leading clinical development for Internal Medicine assets at Pfizer, with end-to-end accountability for designing, executing, and interpreting global clinical trials. The individual will serve as the primary clinical leader on cross-functional teams, shaping development plans, supporting regulatory submissions, and engaging with external stakeholders. A strong emphasis is placed on strategic innovation, team leadership, and therapeutic expertise in obesity and endocrinology.
Design and optimize automated workflows for clinical biomarker testing and sample management using advanced liquid handling platforms and integrated data systems. Lead automation integration, troubleshooting, and digital connectivity across laboratory operations, ensuring compliance and scalability. Support AI-enabled workflows and mentorship within a regulated, innovation-driven environment.
Lead the technical development and implementation of a new labeling and secondary packaging operation at Moderna's Harwell site, ensuring compliance with GxP and safety standards. Establish maintenance strategies, lead capital projects, and drive continuous improvement using engineering excellence principles. Work closely with global teams and support digital integration in a high-growth biotech environment.
This role involves managing the end-to-end clinical supply chain for GSK’s global clinical trials, translating protocols into operational supply strategies, and ensuring timely delivery of investigational products. The Clinical Trial Supply Manager acts as the key liaison between supply operations and study teams, overseeing demand planning, depot management, and compliance across phases I–IV trials. The position emphasizes risk-adjusted, patient-focused planning within a regulated GxP environment.
This role involves managing the end-to-end clinical supply chain for GSK's global R&D clinical trials, from protocol review to study close-out. The Clinical Trial Supply Manager translates study protocols into operational supply strategies, ensures timely delivery of investigational products, and acts as the primary liaison between supply chain and clinical teams. The position requires strong planning, risk management, and cross-functional collaboration to support Phase I–IV trials while maintaining compliance with GxP and regulatory standards.
This role involves leading pharmacovigilance and risk management strategy for GSK’s global pharmaceutical assets, with a focus on patient safety across clinical development and post-marketing phases. The Medical Director will lead safety governance, drive signal detection and risk mitigation, and represent GSK in regulatory discussions. It requires deep expertise in drug safety, cross-functional leadership in a matrix environment, and strategic input into global safety operations.
Develop and execute global regulatory strategies for oncology assets, ensuring compliance and optimal labeling across markets. Collaborate with cross-functional teams and regulatory authorities to support product development and approvals. Drive innovation and process improvements within the regulatory lifecycle.
Develop and execute global regulatory strategies for oncology assets, ensuring compliance and optimal labeling across regions. Collaborate with cross-functional teams to align regulatory plans with development goals and support submissions to health authorities. Focus on innovation, patient impact, and navigating complex regulatory landscapes in a hybrid working environment.
Develop and execute global regulatory strategies for oncology assets, ensuring compliance and optimal product labeling across regions. Collaborate with cross-functional teams and regulatory authorities to support product development and approvals. Drive innovation and process improvements within the regulatory lifecycle.
A senior scientific leadership role focused on pharmacovigilance and safety risk management for GSK's global pharmaceutical assets. The role involves leading safety strategy, evaluating clinical data, and ensuring regulatory compliance across development and post-marketing stages. It requires deep expertise in drug safety, cross-functional leadership, and communication with regulatory authorities.
This role leads global regulatory CMC strategy for mRNA-based medicines, developing and implementing regulatory plans for international submissions. The individual will guide CMC documentation, interact with health authorities, and provide strategic input across product development stages, ensuring compliance with EU and global regulations. The position plays a key part in advancing Moderna’s pipeline of transformative therapeutics across vaccines, oncology, and rare diseases.
This role involves leading CMC regulatory strategies and submissions for international markets, with a focus on mRNA-based products across vaccines, oncology, and rare diseases. The individual will guide global regulatory compliance, interact with health authorities, and support manufacturing and quality teams through regulatory interpretation and change control. It requires deep expertise in CTD-format filings and a proactive approach to managing multi-therapeutic regulatory programs in a fast-paced environment.
