The Principal Scientist role involves working within GSK's Genomic Technologies team to develop and apply advanced methods for analyzing large-scale genetic and genomic data. Responsibilities include collaborating with multidisciplinary teams to identify causal genes, disease mechanisms, and potential drug targets, as well as contributing to the development of best-in-class analytical tools and methodologies.
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.
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 developing, optimizing, and validating molecular bioanalytical assays—such as qPCR, ddPCR, and RNA isolation—to support mRNA-based clinical programs. The scientist will work within GCL0-compliant (GCLP) frameworks to generate pharmacokinetic and pharmacodynamic data, ensuring regulatory compliance and data integrity. Collaboration with cross-functional teams and adoption of digital tools and automation are key to advancing clinical trial execution and analytical processes.
Serves as the physician lead within the oncology clinical development team, providing medical expertise to design, conduct, and interpret clinical studies in hematology oncology. Responsible for medical monitoring, safety oversight, protocol development, and cross-functional collaboration to ensure patient safety and clinical integrity. Engages with investigators and regulatory bodies, contributing to regulatory submissions and scientific communications.
This role involves providing medical leadership in oncology clinical development, with responsibilities spanning study design, medical monitoring, safety oversight, and data interpretation. The Medical Director will integrate physician-level insights into clinical trials, collaborate with cross-functional teams and external experts, and contribute to regulatory submissions and scientific communications. The position emphasizes patient-centered decision-making and real-world impact in cancer treatment innovation.
This role involves leading and executing strategic RWD partnerships to enhance GSK's R&D and commercial activities. Responsibilities include managing data access, ensuring operational execution, and collaborating with internal and external stakeholders to maximize the value of RWD in decision-making and evidence generation.
This role involves leading and executing strategic partnerships for Real World Data (RWD) to support GSK's R&D and commercial activities. Responsibilities include managing data partnerships, ensuring data access and analysis, and collaborating with various internal and external stakeholders to enhance the usability and impact of RWD.
The Medical Director, Oncology Clinical Development - GI, provides medical expertise and oversight for clinical studies, ensuring patient safety and clinical integrity. The role involves leading medical monitoring, interpreting clinical data, and collaborating with cross-functional teams to advance oncology treatments.
This role involves leading the development and deployment of AI solutions to accelerate insights across GSK's commercial operations. Responsibilities include identifying high-value AI opportunities, building business cases, and collaborating with engineering teams to ensure the successful implementation and scaling of AI-driven products.
This role involves leading the generation and dissemination of real-world evidence and health outcomes research for GSK's RSV vaccines. Responsibilities include managing data generation plans, collaborating with cross-functional teams, and engaging with external stakeholders to ensure robust evidence supports product positioning and market access.
This role involves leading the generation and dissemination of real-world evidence and health outcomes research for RSV vaccines. Responsibilities include managing data generation plans, collaborating with cross-functional teams, and engaging with external stakeholders to ensure robust evidence supports vaccine development and commercial success.
This role involves leading the generation and dissemination of real-world evidence and health outcomes research for GSK's RSV vaccines. Responsibilities include managing data generation plans, collaborating with cross-functional teams, and engaging with external stakeholders to ensure robust evidence supports product positioning and market access.
