Biotechnology Jobs

392 jobs for “Pharmaceuticals”

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Director, Cardiovascular and metabolic diseases, Clinical Pharmacology Modeling and Simulation

6 days ago

GSK London US$188,100 – US$313,500 pa

Leads end-to-end Model-Informed Drug Development and clinical pharmacology strategy across the drug development lifecycle, from first-in-human studies through filing and lifecycle management. Sits in the Clinical Pharmacology and Quantitative Medicine organisation, partnering with digital medicine, translational imaging, modelling and data science teams, and drafting regulatory content for FDA, EMA and ICH submissions.

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Director, Cardiovascular and metabolic diseases, Clinical Pharmacology Modeling and Simulation

6 days ago

GSK Stevenage US$188,100 – US$313,500 pa

Lead end-to-end application of Model-Informed Drug Development across the drug development lifecycle, from first-in-human studies through filing and lifecycle management, providing clinical pharmacology strategy and evidence generation. Draft and review regulatory content for FDA, EMA, CDE, PMDA and ICH, and build cross-functional partnerships across digital medicine, translational imaging, AI/ML and biostatistics. The role sits in the newly established Clinical Pharmacology and Quantitative Medicine organisation, reporting into the Respiratory, Immunology & Inflammation Research Unit.

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Vice President - Oncology Clinical Development, Disease Area Head- Hematology

2 weeks ago

GSK London

Leads end-to-end clinical development strategy for a hematology oncology portfolio, from first-in-human studies through registrational trials, regulatory approval and initial launch. Provides program oversight at governance forums, co-leads asset development with matrix partners, and line-manages Clinical Development Leads, Medical Directors and Clinical Scientists. Champions novel approaches such as AI/ML, innovative trial designs and real-world data.

Hybrid
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VP, Medicine Development Leader- Cancer Vaccines, Oncology Research Unit

2 weeks ago

GSK Upper Providence US$340,500 – US$567,500 pa

Leads global development of a cancer vaccine asset from late-stage transition through approval and launch, acting as single point of accountability. Builds and leads a matrix Medicine Development Team spanning clinical development, immunology, manufacturing, regulatory, safety, medical affairs and commercial, and drives strategy, go/no-go decisions and lifecycle planning.

Hybrid
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VP, Medicine Development Leader- Cancer Vaccines, Oncology Research Unit

2 weeks ago

GSK USA - Pennsylvania - Upper Providence US$340,500 – US$567,500 pa

Leads global development of a cancer vaccine asset from late-stage transition through approval and launch, acting as single point of accountability. Builds and directs a matrix Medicine Development Team spanning clinical development, immunology, manufacturing, regulatory, safety, medical affairs and commercial, and drives strategy, go/no-go decisions and lifecycle planning.

Hybrid
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Clinical Development Medical Director - Cardiovascular

Last week

GSK USA - Pennsylvania - Upper Providence US$222,750 – US$371,250 pa

Provides clinical and scientific leadership across cardiovascular clinical development programs, designing CDPs, study protocols and regulatory documents while overseeing medical monitoring and participant safety. Leads a cross-functional Clinical Matrix Team, partners with biology, translational sciences, regulatory and commercial groups, and serves as clinical point of contact for regulators, investigators and key experts. Hybrid role with at least two on-site days per week.

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

2 weeks ago

GSK USA - Pennsylvania - Upper Providence US$204,000 – US$340,000 pa

Leads the design and execution of real-world evidence and health outcomes studies across oncology assets, managing timelines, budgets and vendor deliverables. Reviews protocols, analysis plans and publications, and advises medical, market access and commercial teams on payer and HTA evidence needs. Builds relationships with external experts and maintains knowledge of real-world data sources.

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

2 weeks ago

GSK Baar Onyx US$204,000 – US$340,000 pa

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 deep knowledge of RWD sources and payer evidence needs.

Hybrid
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Senior Medical Director, Oncology Clinical Development - Lung

2 weeks ago

GSK USA - Pennsylvania - Upper Providence US$242,550 – US$404,250 pa

Senior physician leader providing medical oversight, safety monitoring and clinical insight across lung cancer studies, from protocol design through data interpretation. Serves on the Clinical Matrix Team, contributes to regulatory interactions and external scientific engagement, and mentors Medical Directors within the programme. Requires deep lung cancer drug development expertise, including early phase trials.

On-site
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Medical Director, Oncology Clinical Development - Lung & Head/Neck Cancers

2 weeks ago

GSK USA - Pennsylvania - Upper Providence US$222,750 – US$371,250 pa

Serves as the physician within oncology clinical programme teams for lung and head/neck cancers, leading medical monitoring, safety oversight and clinical data interpretation across Phase I–III studies. Partners with a Senior Scientist and cross-functional matrix teams on protocol development, regulatory interactions and investigator engagement, with on-site presence 2–3 days per week.

On-site
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Senior Medical Director, Oncology Clinical Development - GU

2 weeks ago

GSK USA - Pennsylvania - Upper Providence US$284,250 – US$473,750 pa

Leads clinical development of GU oncology assets, designing and executing Phase 1-3 interventional trials and serving as a core member of the Clinical Matrix Team. Provides real-time medical monitoring, safety data review with pharmacovigilance, and authors clinical study reports and regulatory responses. Builds key external expert relationships and contributes to business development diligence.

On-site
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Clinical Development Medical Director- Hepatology

3 weeks ago

GSK Upper Providence US$202,500 – US$371,250 pa

Leads clinical development strategy for hepatology assets within the Respiratory, Immunology & Inflammation Research Unit, from target identification through proof-of-concept studies. Accountable for clinical matrix team leadership, protocol design, medical monitoring and safety governance, and regulatory interactions across all development phases.

Hybrid
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Medical Director, Oncology Clinical Development - GU

2 weeks ago

GSK USA - Pennsylvania - Upper Providence US$189,750 – US$316,250 pa

Serves as the physician within a clinical program team, leading medical monitoring and safety oversight for genitourinary oncology studies. Interprets clinical and safety data, contributes to protocol development and regulatory interactions, and acts as a core member of the Clinical Matrix Team. May guide other physicians on complex multi-study programs.

Hybrid
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Medical Director Clinical Development- Aging

3 weeks ago

GSK USA - Pennsylvania - Upper Providence US$189,750 – US$316,250 pa

Provides clinical and scientific leadership across translational and clinical studies within GSK's Respiratory, Immunology & Inflammation Research Unit, focusing on aging. Leads the Clinical Matrix Team, designs clinical development plans and protocols, oversees medical monitoring and safety, and drives regulatory interactions. Works cross-functionally with biology, regulatory, commercial and statistics to advance assets from early development.

Hybrid
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Medical Director-Oncology Clinical Development - GI

2 weeks ago

GSK USA - Pennsylvania - Upper Providence US$222,750 – US$371,250 pa

Serves as the physician within an oncology clinical programme team, leading medical monitoring and safety oversight for GI cancer studies. Interprets clinical and safety data, contributes to protocol development, and engages investigators, KEEs and health authorities. A core member of the Clinical Matrix Team, providing medical guidance within a matrixed pharma R&D environment.

On-site

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