Latest Healthcare Jobs

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

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

(Fixed-Term) Manufacturing Associate I

Operate and maintain equipment in a cGMP-compliant, highly automated mRNA vaccine production environment at Moderna's Oxford facility. Perform production operations, support quality assurance, troubleshoot issues, and contribute to continuous improvement initiatives using digital systems and advanced manufacturing technologies. Work within a 2-2-3 rotating shift pattern to ensure reliable, safe, and compliant vaccine manufacturing.

Moderna Oxford, United Kingdom

Scientist, Clinical Biomarker Laboratory, Immuno-Assays - Cell Based

This role involves leading the development, qualification, and execution of complex cell-based immunoassays to support Moderna’s clinical trials across multiple therapeutic areas. The scientist will generate high-quality, regulatory-compliant data using advanced immunological techniques and serve as a subject matter expert within cross-functional teams. Emphasis is placed on innovation, scientific rigor, and integration of emerging technologies including digital and AI-enabled workflows in a GCP/GLP-regulated environment.

Moderna

Hybrid Permanent

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

Principal Safety Scientist - SERM

This role involves leading safety evaluation and risk management for GSK's clinical and post-marketing products. Responsibilities include signal detection, authoring safety reports, and collaborating with cross-functional teams to ensure patient safety globally.

GSK

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

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

Principal Safety Scientist - SERM

This role involves providing medical and scientific expertise in the safety evaluation and risk management of GSK products, both in clinical development and post-marketing. Responsibilities include leading signal detection, authoring safety reports, and collaborating with cross-functional teams to ensure patient safety.

GSK £215,250 – £358,750 pa

Principal Safety Scientist - SERM

This role involves providing medical and scientific expertise in the safety evaluation and risk management of GSK products, both in clinical development and post-marketing. Responsibilities include signal detection, safety documentation, and cross-functional collaboration to ensure patient safety globally.

GSK

Principal Safety Scientist - SERM

This role involves leading safety evaluation and risk management for GSK products in clinical development and post-marketing. Responsibilities include signal detection, authoring safety reports, and collaborating with cross-functional teams to ensure patient safety globally.

GSK £215,250 – £358,750 pa

Principal Safety Scientist - SERM

This role involves providing medical and scientific expertise in the safety evaluation and risk management of GSK products, both in clinical development and post-marketing. Responsibilities include leading signal detection, authoring safety reports, and collaborating with cross-functional teams to ensure patient safety globally.

GSK

Principal Safety Scientist - SERM

This role involves leading safety evaluation and risk management for GSK products in clinical development and post-marketing. Responsibilities include signal detection, safety documentation, and cross-functional collaboration to ensure patient safety globally.

GSK

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

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