Latest Pharmaceuticals Jobs

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Medical Director, Oncology Clinical Development

Leads clinical development of oncology assets through trial design, execution, and data interpretation, ensuring scientific integrity and regulatory compliance. Engages with external experts and cross-functional teams to advance GSK’s oncology pipeline. Focuses on generating robust clinical evidence to support approvals and lifecycle management.

GSK United States
Hybrid Permanent
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Medical Director, Oncology Clinical Development

This role involves leading clinical research activities for GSK’s oncology portfolio, including designing and executing phase 1-3 trials, ensuring scientific integrity, and supporting regulatory submissions. The Medical Director will collaborate with internal and external experts to advance clinical development strategies and drive data generation in oncology. The position requires strong medical and scientific leadership in a matrix environment with a focus on patient impact.

GSK
Hybrid Permanent
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Senior Director, Targets and Mechanisms Solutions

Leads the strategic direction and AI-driven innovation of Pfizer's Targets and Mechanisms platforms, overseeing a global team to deliver scalable, science-centric digital solutions for drug discovery. Focuses on integrating advanced technologies like AI, data pipelines, and predictive analytics to support target identification, translational research, and preclinical strategy across therapeutic areas. Works closely with R&D and digital teams to align technology roadmaps with research objectives and drive enterprise-scale delivery.

Pfizer £230,900 – £384,800 pa
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Global Development Lead, Internal Medicine, Sr. Director (MD)

This role involves leading clinical development for Internal Medicine assets within Pfizer's Research & Development division, with end-to-end accountability for creating and executing global clinical development plans. The position requires deep therapeutic expertise in chronic weight management or endocrinology, leadership of cross-functional teams, and active engagement in trial design, regulatory submissions, and lifecycle strategy. The role operates in a hybrid work model and may include responsibilities across the Obesity portfolio.

Pfizer United States £274,500 – £457,500 pa
On-site Permanent
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Medical Director Clinical Development- Respiratory

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.

GSK
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Medical Director, Oncology Clinical Development - Hematology

The Medical Director, Oncology Clinical Development - Hematology is a physician-led role focused on guiding clinical strategy and medical oversight in oncology drug development. This position involves leading medical monitoring, interpreting clinical and safety data, contributing to protocol design, and engaging with investigators and regulatory bodies. The role operates within cross-functional teams to ensure patient safety and clinical integrity across Phase I–III trials in hematology and oncology.

GSK United States
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Medical Director, Oncology Clinical Development - Hematology

This role involves leading medical oversight in oncology clinical development, focusing on hematology. The Medical Director will guide study design, ensure patient safety, interpret clinical data, and collaborate with cross-functional teams and external experts. It emphasizes physician leadership in trials from Phase I–III, with a strong focus on real-world impact and regulatory engagement.

GSK £222,750 – £371,250 pa
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Medical Director, Oncology Clinical Development - Hematology

This role involves leading medical oversight and clinical development for oncology and hematology programs, with responsibilities spanning study design, safety monitoring, data interpretation, and regulatory engagement. The Medical Director will collaborate with cross-functional teams and external experts to ensure clinical integrity and patient-centered decision-making in late-stage drug development. The position requires deep expertise in hematology-oncology and experience in Phase I–III trials within a pharmaceutical or biotech setting.

GSK PLN 455,250 – PLN 758,750 pa
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Medical Director, Oncology Clinical Development - Hematology

Serves as the physician lead within the oncology clinical development team, providing medical expertise to design, conduct, and interpret clinical studies in hematology oncology. Responsible for medical monitoring, safety oversight, protocol development, and cross-functional collaboration to ensure patient safety and clinical integrity. Engages with investigators and regulatory bodies, contributing to regulatory submissions and scientific communications.

GSK
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Medical Director, Oncology Clinical Development - GU

This role involves providing medical leadership within oncology clinical development, specifically in genitourinary (GU) cancers. The Medical Director will lead medical monitoring, ensure patient safety, contribute to study design and regulatory interactions, and interpret clinical data to inform decision-making. They will work closely with cross-functional teams and external experts to advance GSK’s oncology pipeline with a focus on high unmet need areas.

GSK Switzerland
Hybrid Permanent
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Medical Director, Oncology Clinical Development - GU

This role involves leading medical oversight and clinical strategy for genitourinary (GU) oncology trials within GSK’s R&D pipeline. The Medical Director provides physician-level expertise in study design, safety monitoring, data interpretation, and regulatory engagement, ensuring patient safety and scientific integrity. They collaborate with cross-functional teams and external experts to advance innovative cancer treatments through clinical development.

GSK £189,750 – £316,250 pa
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Medical Director, Oncology Clinical Development - GU

This role involves leading medical strategy and oversight for genitourinary (GU) oncology clinical trials within GSK’s R&D pipeline. The Medical Director provides physician-level expertise in study design, real-time safety monitoring, data interpretation, and regulatory engagement, ensuring patient safety and clinical integrity. They work cross-functionally within a matrix team to advance innovative cancer therapies from development through to regulatory submission and scientific dissemination.

GSK £189,750 – £316,250 pa
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Medical Director, Oncology Clinical Development - GU

This role involves providing medical leadership within oncology clinical development for genitourinary (GU) cancers, focusing on study design, medical monitoring, and safety oversight. The physician will interpret clinical and safety data, contribute to regulatory submissions, and engage with investigators and external experts. Working within a cross-functional team, the role ensures patient safety and clinical integrity across trials while supporting GSK’s mission to advance innovative cancer treatments.

GSK
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Medical Director, Oncology Clinical Development - GU

This role involves providing medical leadership in oncology clinical development for genitourinary (GU) cancers, with responsibility for medical monitoring, safety oversight, and clinical data interpretation across trials. The Medical Director integrates physician expertise into study design, regulatory interactions, and cross-functional decision-making, working within a global matrix team. The position requires deep oncology knowledge, experience in clinical trial conduct, and strong collaboration with internal teams and external experts.

GSK
GSK logo

Medical Director, Oncology Clinical Development - GU

This role involves providing medical leadership in oncology clinical development, specifically for genitourinary (GU) cancers. The Medical Director will lead medical monitoring, contribute to protocol design, interpret clinical data, and ensure patient safety across clinical trials. They will work closely with cross-functional teams, engage with external experts, and support regulatory submissions and scientific communications within a global pharmaceutical environment.

GSK
Hybrid Permanent