Future Tech Jobs
Future Tech Jobs
Interventional Study Scientist Medical DirectorLocations– GSK HQ UK, New Oxford Street & USA - Upper Providence/ Waltham MAReports to: Head of Interventional & Supported StudiesJoin GSK's Medical Affairs team and be part of a global organization that drives innovation, scientific...
The Director Medical Writing Process Management will lead the optimization of end-to-end business processes within Medical Writing, ensuring compliance, efficiency, and continuous improvement. They will collaborate with cross-functional teams to implement best practices, monitor process health, and align with GSK’s strategic goals.
This role involves developing and refining processes, risk management strategies, and other activities essential to the success of the Global Collaborative Studies Group (CSG) at ViiV Healthcare. You will lead the Request for Proposal study process, manage study-related activities, and work cross-functionally with various teams to ensure timely and compliant delivery of supported studies.
Leads end-to-end CMC and supply chain strategy for a physical medicine from pre-clinical development through commercialisation, including process development, regulatory filings, and lifecycle planning. Works across global matrix teams to deliver robust manufacturing processes, ensure PAI readiness, and transition responsibilities to commercial operations. Focuses on complex products such as small molecules or oligonucleotides, integrating technical, regulatory, and supply considerations.
This role involves leading global medical strategy in hepatology, shaping evidence generation and scientific communication plans, and collaborating across R&D, regulatory, and market access teams. The position drives patient-focused medical initiatives, ensures robust scientific training, and optimizes external engagement with healthcare professionals, payors, and regulators. It offers leadership growth within a therapy area poised for innovation.
Lead the development and execution of global medical strategy in hepatology, aligning with local market needs and driving evidence generation and scientific communication. Collaborate across R&D, regulatory, and market access teams to optimize clinical care and deliver impactful medical plans. Build relationships with key stakeholders including healthcare professionals, patients, and regulators to advance patient-centred outcomes.
This role involves providing end-to-end technical leadership for a pharmaceutical product throughout its lifecycle, from development through manufacturing and commercial supply. The Molecule Steward ensures product quality, process robustness, and regulatory compliance by leading technical strategy, coordinating cross-functional teams, and driving continuous improvement across global supply chain sites. The position requires deep scientific expertise, strong leadership in matrixed environments, and active involvement in regulatory submissions and lifecycle management.
This role involves end-to-end technical leadership for a pharmaceutical product across its lifecycle, from development through manufacturing and commercialization. The Molecule Steward ensures product quality, robustness, and compliance by leading technical strategy, process optimization, and cross-functional collaboration across R&D, manufacturing, and regulatory teams. They play a key role in technology transfer, continuous process verification, and maintaining control strategies in a highly regulated environment.
This role involves providing end-to-end technical leadership for a pharmaceutical product across its lifecycle, from development through manufacturing and commercialization. The Molecule Steward ensures product quality, regulatory compliance, and process robustness by leading cross-functional teams, defining control strategies, and driving continuous improvement initiatives. It requires deep scientific expertise, strong leadership in matrixed environments, and coordination across R&D, manufacturing, and regulatory functions.
This role involves providing end-to-end technical leadership for a pharmaceutical product throughout its lifecycle, from development to commercial manufacturing. The Molecule Steward ensures product quality, robustness, and manufacturability by leading technical strategy, process optimization, and regulatory compliance across global supply chain teams. The position requires deep scientific expertise, cross-functional collaboration, and leadership in resolving complex technical challenges in a regulated environment.
This role involves collaborating with internal and external stakeholders to support the commercial manufacture of large molecule drug substances and sterile drug products. Responsibilities include executing technical strategies, managing product lifecycle activities, and ensuring compliance with GMP standards. The role also involves supporting CMOs in audits, technical transfers, and continuous improvement initiatives.
This role involves collaborating with internal and external stakeholders to support the commercial manufacture of large molecule drug substances and sterile drug products. Responsibilities include executing technical strategies, providing lifecycle support, and ensuring compliance with GMP standards. The role also focuses on continuous improvement and managing technical transfers between contract manufacturing organizations (CMOs).
This role involves leading the global medical strategy for a lung cancer asset, working with cross-functional teams to translate scientific insights into practical patient impact. Responsibilities include chairing a global medical team, managing external partnerships, and ensuring scientific quality and compliance.
This role involves leading the global medical strategy for a lung cancer asset, working with cross-functional teams to translate scientific insights into practical patient impact. Responsibilities include chairing a global medical team, managing partnerships with academic centers, and ensuring scientific quality and compliance.
This role involves collaborating with internal and external stakeholders to support the commercial manufacture of large molecule drug substances and sterile drug products. Responsibilities include executing technical strategies, managing product lifecycle activities, and ensuring compliance with GMP standards. The position also involves supporting CMOs in audits, technical transfers, and continuous improvement initiatives.
