Latest Therapeutics Jobs

Interventional Study Scientist Medical Director

Leads the scientific design and execution of interventional clinical studies within Medical Affairs, providing medical governance, safety data review and scientific oversight of protocols and analysis plans. Collaborates with cross-functional teams, investigators and thought leaders, and presents results for publications and regulatory submissions. Hybrid role with two to three days per week in office.

GSK London US$187,275 – US$312,125 pa

Hybrid

Interventional Study Scientist Medical Director

Leads the scientific design and execution of interventional clinical studies within Medical Affairs, providing medical governance, safety data review and scientific oversight of protocols and analysis plans. Collaborates with cross-functional teams, investigators and thought leaders, and presents results for publications and regulatory submissions. Hybrid role with two to three days per week in office.

GSK Waltham, United States US$187,275 – US$312,125 pa

Hybrid

Clinical Development Senior Medical Director - Cardiovascular

Leads clinical development medical activities for cardiovascular and vascular programs across early and late-phase studies, shaping clinical development plans, study designs and translational strategies. Serves as clinical lead for a matrix team, providing medical monitoring, regulatory input and safety oversight while working with biology, regulatory, commercial and operations colleagues.

GSK London US$284,625 – US$474,375 pa

Hybrid

Clinical Development Medical Director - Cardiovascular

Provides clinical and scientific leadership across cardiovascular clinical development programmes, shaping study designs, translational plans and regulatory documents within the Respiratory, Immunology & Inflammation Research Unit. Leads a Clinical Matrix Team, oversees participant safety and medical monitoring, and works cross-functionally with biology, regulatory, statistics and commercial partners. Hybrid working with at least two days per week on-site.

GSK London US$222,750 – US$371,250 pa

Hybrid

Clinical Development Medical Director - Cardiovascular

Leads clinical development strategy for cardiovascular assets within the Respiratory, Immunology & Inflammation Research Unit, designing clinical development plans, protocols and regulatory documents while providing medical monitoring and safety oversight. Chairs the Clinical Matrix Team and serves as primary clinical contact for regulators, investigators and key external experts across early and late-stage programs.

GSK Waltham, United States US$222,750 – US$371,250 pa

Hybrid

Clinical Development Medical Director - Cardiovascular

Provides clinical and scientific leadership across early-phase cardiovascular programs, shaping clinical development plans, study designs and regulatory documents. Leads a cross-functional Clinical Matrix Team, oversees medical monitoring and safety, and acts as the clinical point of contact for regulators, investigators and key external experts. Hybrid role with at least two days per week on-site.

GSK Stevenage US$222,750 – US$371,250 pa

Hybrid

SERM Medical Director

Provides medical and scientific leadership for pharmacovigilance and risk management of oncology assets in clinical development, interpreting safety data, detecting signals and delivering benefit-risk recommendations. Represents Safety on cross-functional matrix teams and governance committees, and interacts with regulators. Hybrid UK-based role with mentoring and process-improvement duties.

GSK London

Hybrid

SERM Medical Director

Provides medical and scientific leadership for pharmacovigilance and risk management of oncology assets in clinical development, interpreting safety data, detecting signals and delivering benefit-risk recommendations. Represents Safety on cross-functional clinical matrix teams and governance committees, and may lead Safety Review Teams. Hybrid role based in the UK with global regulatory and partner interaction.

GSK Wavre, Belgium

Hybrid

Finance Portfolio Analytics Analyst

Builds and maintains financial and valuation models (NPV/rNPV, scenario and sensitivity analysis) and portfolio forecasts, metrics and KPI dashboards for R&D investment decisions. Runs probabilistic and Monte Carlo simulations, cleans data from scientific, clinical, financial and operational sources, and prepares decision materials for portfolio reviews. Works with the Head of Data Science and the Finance Portfolio Analytics Manager in a hybrid, high-visibility team.

GSK USA - Pennsylvania - Upper Providence

Hybrid

Senior, Forward Deployed / Full Stack Engineer (Document Authoring & Knowledge Systems)

Embedded forward deployed engineer role in GSK's Enterprise AI team, working within the Chemical Manufacturing & Control area to prototype AI solutions at days-to-weeks cadence. Focuses on document authoring and generation for regulatory filings, agentic workflows, RAG, knowledge systems and LLM evaluation, with heavy daily use of AI coding agents. Proven prototypes are handed off to a Sr. Solutions Engineer for scale-up.

GSK London

Hybrid

Senior, Forward Deployed / Full Stack Engineer (Document Authoring & Knowledge Systems)

Embedded with CMC business teams, you take high-priority AI use cases from problem framing to working prototypes at days-to-weeks cadence, then ship first production versions. The work centres on document authoring and generation for regulatory filings, building agentic and RAG pipelines, human-in-the-loop review workflows, and LLM evaluation with golden datasets and regression testing.

GSK Stevenage

Hybrid

Principal Medical Writer

Lead authoring and strategic planning for clinical and regulatory documents, including protocols, clinical study reports, briefing documents and submission dossiers. Manages end-to-end writing projects, coordinating contributors, timelines and quality checks, and acts as subject matter expert on medical writing standards, CTD structure and regulatory expectations while driving process improvement and audit readiness.

GSK Durham, United States

Principal Medical Writer

Lead authoring and strategic planning of clinical and regulatory documents such as protocols, clinical study reports, briefing documents and CTD submission dossiers. Manage end-to-end writing projects, coordinating contributors, timelines and quality checks, and act as subject matter expert on medical writing standards and regulatory expectations while driving process improvement and audit readiness.

GSK London

Director, Global Real-World Evidence & Health Outcomes Scientist, Oncology

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.

GSK Waltham, United States US$204,000 – US$340,000 pa

Hybrid

Director, Global Real-World Evidence & Health Outcomes Scientist, Oncology

Leads the design and execution of real-world evidence and health outcomes studies across 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, while building knowledge of real-world data sources and payer needs.

GSK London US$204,000 – US$340,000 pa

Hybrid