494 jobs for “Clinical Research Physician”
Serves as the physician on a clinical program team, leading medical monitoring and safety oversight for oncology and hematology studies. Interprets clinical and safety data, contributes to protocol development, and engages investigators, regulators and cross-functional matrix teams. May guide other physicians on complex multi-study programs.
AI
Serves as the physician on a clinical program team, leading medical monitoring and safety oversight for oncology and hematology studies. Interprets clinical and safety data, contributes to protocol development, and engages with investigators, regulators, and cross-functional matrix teams. May guide other physicians on complex multi-study programs.
AI
Leads precision diagnostics strategy for oncology programmes, defining diagnostic requirements for trials and overseeing biomarker selection, assay validation and sample handling. Manages project plans, budgets and timelines while engaging diagnostic companies, clinical labs and vendors, and supporting regulatory submissions. Works cross-functionally with research, clinical, regulatory and commercial teams in a hybrid model.
FDA · EU IVDR · PMDA +2
Leads precision diagnostics strategy for oncology programmes, defining biomarker selection, assay validation and sample collection across multiple assets. Oversees project plans, budgets and regulatory submissions while managing external diagnostic partners and clinical labs. Hybrid role based in Stevenage, relocating to Cambridge by early 2029.
FDA · EU IVDR · PMDA/MHLW Japan +2
Leads precision diagnostics strategy for oncology programs, defining diagnostic requirements for trials and overseeing biomarker selection, assay validation, and sample collection. Partners cross-functionally with research, clinical, regulatory, and commercial teams, and engages external diagnostic companies and labs to accelerate assay development. Hybrid role based in Waltham, MA.
FDA · EU IVDR · PMDA/MHLW Japan +2
GSK · 10000+ people · Public
Provides scientific and strategic leadership for real-world evidence supporting an mRNA vaccine portfolio, with a primary focus on influenza. Shapes evidence generation across late-stage development, launch and post-marketing, leading US post-marketing vaccine effectiveness studies and external academic and data-partner collaborations. Requires deep expertise in influenza epidemiology, real-world data and causal methods, plus influence across a global matrix.
Medicare · EHR
GSK · 10000+ people · Public
Provides scientific and strategic leadership for real-world evidence supporting an mRNA vaccine portfolio, with a primary focus on influenza. Shapes evidence generation across late-stage development, launch and post-marketing, leading US post-marketing vaccine effectiveness studies and complex external collaborations with academic and healthcare data partners.
Medicare · EHR · Administrative Claims +1
GSK · 10000+ people · Public
Provides scientific and strategic leadership for real-world evidence supporting an mRNA vaccine portfolio, with a primary focus on influenza. Shapes evidence generation across late-stage development, launch and post-marketing phases, leading US post-marketing vaccine effectiveness studies and complex external collaborations with academic and healthcare data partners.
Medicare · EHR · Administrative Claims +1
GSK · 10000+ people · Public
Leads the integrated real-world evidence and health outcomes strategy for mRNA influenza vaccines, designing and interpreting US post-marketing vaccine effectiveness studies across late-stage development, launch and post-marketing phases. Partners with clinical development, epidemiology, medical affairs, regulatory, biostatistics and market access teams, and builds collaborations with academic investigators, healthcare systems and data partners. Requires deep expertise in US vaccine effectiveness research, influenza epidemiology, real-world data and causal methods.
Medicare · EHR · Administrative Claims +1
Leads precision diagnostics strategy for oncology programmes, defining diagnostic requirements for trials, biomarker selection, assay validation and sample handling. Oversees project plans, budgets and regulatory submissions while managing external diagnostic partners, labs and vendors in a matrixed cross-functional environment.
FDA · EU IVDR · PMDA/MHLW Japan +2
GSK · 10000+ people · Public
Provides scientific and strategic leadership for real-world evidence supporting GSK's mRNA vaccine portfolio, with a primary focus on influenza. Leads post-marketing vaccine effectiveness studies in the US, translating evidence needs into rigorous study designs and building collaborations with academic investigators, healthcare systems and data partners. Requires deep expertise in US vaccine effectiveness research, influenza epidemiology, real-world data and causal methods.
Medicare · EHR
GSK · 10000+ people · Public
Leads global medical writing for the Respiratory, Immunology and Inflammation portfolio, directing strategy, resourcing and delivery of regulatory-compliant clinical documentation to accelerate submissions. Drives innovation and digital/AI adoption, manages vendor oversight and talent development, and partners with senior R&D stakeholders on governance and process improvement.
AI · Content Management Systems
Owns the product vision and roadmap for AI-enabled digital products that support structured, collaborative authoring of evidence and regulatory content across clinical, non-clinical, CMC, safety, regulatory and publications. Leads a multi-disciplinary product team, shapes scalable architecture with engineers, and drives an AI-first approach with GxP, privacy and AI governance embedded from the outset.
Cloud · DevOps
GSK · 10000+ people · Public
Leads global medical writing for the Respiratory, Immunology and Inflammation portfolio, directing strategy, resource planning and vendor oversight to deliver regulatory-compliant clinical documentation. Drives submission acceleration, digital innovation and cross-functional partnerships across R&D, with accountability for talent development and operational excellence.
Content Management Systems
GSK · 10000+ people · Public
Leads the design and execution of real-world evidence and health outcomes studies for oncology assets, managing timelines, budgets and quality of protocols, analyses and publications. Advises internal medical, market access and commercial teams and external experts on evidence strategy for HTA submissions, reimbursement and value-based pricing. Requires close collaboration across a matrix and deep knowledge of real-world data sources and payer needs.
