Future Tech Jobs
Future Tech Jobs
This role involves leading the generation of strategic insights for a key oncology brand within GSK's ADC portfolio. Responsibilities include shaping commercial forecasts, conducting global market research, and partnering with cross-functional teams to drive business strategy and competitive intelligence.
The Project Manager for External Manufacturing-Drug Substance (EM-DS) leads technical transfer projects to external CMO partners, ensuring timely and budgeted delivery. Key responsibilities include managing cross-functional teams, mitigating risks, and maintaining strong relationships with suppliers and internal stakeholders.
The Global Development Lead (GDL) is responsible for leading the clinical development of assigned assets in Internal Medicine. This involves designing, executing, and interpreting clinical studies, creating development plans, and collaborating with cross-functional teams to ensure regulatory approvals and global market access. The role also includes specialized monitoring, regulatory submissions, and engaging with external stakeholders to drive strategic insights.
The Global Development Lead (GDL) is responsible for leading the clinical development of assigned assets in Internal Medicine, working closely with cross-functional teams to design, execute, and interpret clinical studies. Key responsibilities include creating clinical development plans, regulatory submissions, and providing expert input on trial design and execution, while ensuring compliance and strategic insight generation.
This role involves leading Chemistry, Manufacturing and Controls (CMC) regulatory activities across development, registration, and early lifecycle stages. You will work with cross-functional teams to develop regulatory strategies, prepare submissions, and provide regulatory advice, while also mentoring colleagues and improving processes.
This role involves leading Chemistry, Manufacturing and Controls (CMC) regulatory activities across development, registration, and early lifecycle stages. You will work with cross-functional teams to develop regulatory strategies, prepare submissions, and provide regulatory advice, while also mentoring colleagues and contributing to process improvements.
The Senior Director, Respiratory Innovation, will lead a team of epidemiologists in conducting and overseeing advanced epidemiologic studies and real-world evidence generation. This role involves strategic leadership, team development, and collaboration with cross-functional teams to support the research and development of vaccines and infectious diseases.
The Senior Director, Respiratory Innovation, will lead a team of epidemiologists in conducting and overseeing advanced epidemiologic studies and real-world evidence generation for respiratory diseases. This role involves strategic leadership, team development, and collaboration with cross-functional teams to support vaccine and infectious disease R&D.
The Senior Director, Respiratory Innovation, will lead a team of epidemiologists in conducting advanced research and studies on respiratory diseases, leveraging real-world data and cutting-edge methods. This role involves strategic leadership, team development, and collaboration with cross-functional teams to support vaccine and infectious disease R&D programs.
The Senior Director, Respiratory Innovation, will lead a team of epidemiologists in conducting advanced epidemiologic studies and real-world evidence generation for respiratory diseases. This role involves strategic leadership, team development, and collaboration with cross-functional teams to support vaccine and infectious disease R&D.
The Senior Director, Respiratory Innovation, will lead a team of epidemiologists in conducting advanced epidemiologic studies and real-world evidence generation for respiratory diseases. This role involves strategic leadership, team development, and collaboration with cross-functional teams to support vaccine and infectious disease R&D.
This role involves defining and leading the European commercial strategy for GSK’s lung oncology portfolio, ensuring alignment with global strategies and driving successful product launches across multiple European markets. Key responsibilities include performance management, cross-functional collaboration, and ensuring patient access to GSK medicines.
This role involves leading Chemistry, Manufacturing and Controls (CMC) regulatory activities across development, registration, and early lifecycle stages. You will work with cross-functional teams, provide regulatory advice, and support inspections and quality events. The position offers opportunities for growth through complex regulatory work and direct impact on patient health.
This role involves leading Chemistry, Manufacturing and Controls (CMC) regulatory activities across development, registration, and early lifecycle stages. You will work with cross-functional teams, provide regulatory advice, and manage interactions with regulatory authorities, ensuring compliance and supply continuity.
This role involves working with internal and external labs to ensure E&L testing is completed scientifically and compliantly. Responsibilities include conducting risk assessments, delivering technical information, and managing risk identification for biopharmaceutical manufacturing processes and packaging systems.
