Leads clinical development for respiratory assets, designing and executing clinical and translational strategies to advance drug candidates. Provides medical oversight, contributes to regulatory submissions, and collaborates across functions to deliver innovative medicines. Focuses on patient-centric innovation and scientific rigor in a matrix environment.
Lead clinical development strategy and execution for hepatology assets within GSK’s Respiratory, Immunology & Inflammation Research Unit. Provide medical oversight across translational and clinical studies, design development plans and protocols, and guide decision-making for early-phase programs. Work cross-functionally to advance novel liver disease treatments from discovery through clinical proof of concept, leveraging biomarker and real-world data to inform development.
Leads clinical development for assigned assets in Internal Medicine, driving global clinical strategy, trial design, execution, and regulatory submissions. Serves as primary clinical accountability, collaborating with cross-functional teams and external stakeholders to advance drug development programs from concept through approval, with potential focus on obesity-related therapeutics.
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 developing, validating, and executing ligand-binding and cell-based assays to support mRNA medicine development. The candidate will generate pharmacodynamic and immunogenicity data in a regulated GcLP environment, manage critical reagent characterization, and contribute to clinical sample testing using Watson LIMS. The position emphasizes scientific rigor, regulatory compliance, and collaboration within a high-performance team advancing novel bioanalytical assays.
This role involves leading the creation and management of investigator site budgets and contracts for clinical trials, using Grants Manager and FMV benchmarking tools. The candidate will oversee CRO activities, ensure budget consistency across trials, and support timely site activation by managing negotiations and identifying risks. Collaboration with legal, clinical operations, and external partners is central to ensuring compliance and efficiency in contract execution.
This role involves leading pharmacovigilance and risk management strategy for GSK's global assets, with a focus on safety evaluation in immunology and other therapeutic areas. The Scientific Director will lead safety governance, contribute to regulatory submissions, and manage cross-functional teams to address product safety issues. They will also represent GSK in interactions with regulatory authorities and ensure compliance with global pharmacovigilance standards.
Develops and executes global regulatory strategies for oncology products, ensuring compliance and optimal labeling across markets. Collaborates with cross-functional teams and regulatory authorities to support product development and approvals. Focuses on innovation, patient impact, and strategic decision-making within a matrix environment.
Develop and execute global regulatory strategies for oncology assets, ensuring compliance and optimal 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 framework.
Develops and executes global regulatory strategies for oncology products, ensuring compliance and optimal labeling across regions. Collaborates with cross-functional teams and regulatory authorities to support product development and approvals. Focuses on strategic planning, regulatory intelligence, and process innovation within a patient-first framework.
Develops and executes global regulatory strategies for oncology products, ensuring compliance and optimal labeling across markets. Collaborates with cross-functional teams and regulatory authorities to support product development and approvals. Focuses on innovation, patient impact, and strategic alignment within a matrix environment.
This role involves managing the end-to-end clinical supply chain for global clinical trials, translating study protocols into operational supply strategies, and ensuring timely, compliant delivery of investigational products. The Clinical Trial Supply Manager acts as the primary link between supply chain and clinical teams, overseeing demand planning, inventory policies, depot coordination, and risk mitigation across Phase I–IV studies. Key responsibilities include maintaining supply plans, managing external partners, and driving continuous improvement in supply processes.
This role involves developing and executing global and regional regulatory strategies for oncology products across their lifecycle, ensuring compliance and optimal labeling. The manager will collaborate with cross-functional teams and regulatory authorities to support submissions and approvals, leveraging regulatory intelligence to inform decision-making. The position emphasizes strategic planning, stakeholder engagement, and innovation within a patient-focused biopharma environment.
This role involves managing the end-to-end clinical supply chain for 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 chain and clinical teams, overseeing demand planning, depot management, and compliance across phases I–IV studies. The position emphasizes risk-adjusted, patient-focused planning and continuous improvement in supply operations.
Manages end-to-end clinical trial supply chains for GSK's global R&D studies, translating protocols into operational supply strategies, ensuring timely delivery of investigational products, and maintaining compliance across phases I–IV. Acts as the primary liaison between clinical teams and supply operations, overseeing demand planning, distribution, and inventory policies while mitigating risks and driving continuous improvement in supply chain performance.
