Latest Healthcare Jobs

Executive Medical Director, Clinical Development Lead - Oncology

Leads clinical development strategy for oncology assets, defining the scientific narrative and benefit-risk framework across the lifecycle. Acts as the primary clinical authority, shaping strategic direction and governance decisions while leveraging AI and advanced analytics to accelerate development. Represents Clinical Development in internal and external forums, including regulatory interactions and alliance partnerships.

GSK US$242,250 – US$403,750 pa

Hybrid Permanent

Executive Medical Director, Clinical Development Lead - Oncology

This role leads the clinical development strategy for oncology assets at GSK, defining the scientific narrative, benefit-risk framework, and decision-making roadmap across the asset lifecycle. The Executive Medical Director serves as the primary clinical authority within the Medicine Development Team, shaping strategic governance, regulatory engagement, and evidence generation. They drive innovation through AI-enabled insights and advanced analytics while mentoring clinical talent and ensuring alignment across regulatory, commercial, and medical functions.

GSK US$242,250 – US$403,750 pa

Hybrid Permanent

(Fixed-Term) Manufacturing Associate I

This role involves operating and maintaining equipment in a cGMP-regulated mRNA vaccine production environment, ensuring safe and compliant manufacturing processes. The associate will execute production operations, support quality assurance, troubleshoot technical issues, and contribute to continuous improvement initiatives. Work is conducted in a highly automated, digitally enabled facility with a focus on operational excellence and innovation in mRNA technology.

Moderna

Senior Manager, Packaging Engineering

Lead the technical development and implementation of a new labeling and secondary packaging operation at Moderna’s Harwell site, from initial design through commissioning and validation. Establish maintenance strategies, ensure GMP compliance, and drive continuous improvement using engineering excellence principles and digital tools. Build and lead a high-performing engineering team to support long-term operational success in a regulated biotech environment.

Moderna

Hybrid Permanent

Global Development Lead, Internal Medicine, Sr. Director (non-MD)

This role leads clinical development for Internal Medicine assets within Pfizer's Research & Development division, serving as the primary clinical accountability point for global regulatory submissions. The individual will direct cross-functional teams in designing and executing Phase 1-3 trials, develop clinical development plans, and contribute to regulatory filings, safety reports, and product labeling. The position emphasizes leadership in obesity-related therapeutics, digital innovation in clinical development, and engagement with external scientific and regulatory stakeholders.

Pfizer

On-site Permanent

Global Development Lead, Internal Medicine, Sr. Director (non-MD)

This role involves leading clinical development for Internal Medicine assets within Pfizer's Research & Development division, with a focus on obesity and chronic weight management. The Global Development Lead is responsible for end-to-end clinical strategy, including designing and executing global clinical trials, regulatory submissions, and cross-functional team leadership. The position requires deep therapeutic expertise, strategic input into product development, and engagement with external stakeholders such as advisory boards and regulatory bodies.

Pfizer US$214,900 – US$358,100 pa

On-site Permanent

Labelling Strategy and Development, Oncology Team Lead

Leads a global labelling team for oncology products, shaping clear, compliant, and patient-focused product labels. Interfaces with regulatory authorities and cross-functional stakeholders to drive labelling strategy and governance. Focuses on aligning regulatory, scientific, and commercial objectives across the oncology portfolio.

GSK

Hybrid Permanent

Medical Director, Oncology Clinical Development

This role involves leading oncology clinical trials from protocol design to study reporting, ensuring scientific integrity and alignment with regulatory and commercial goals. The Medical Director will collaborate with global experts and internal teams to advance GSK’s oncology pipeline, with a focus on data generation, safety monitoring, and strategic medical input across the clinical development lifecycle.

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

Hybrid Permanent

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

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

Medical Director, Oncology Clinical Development

This role involves leading clinical development activities for oncology assets, including designing and executing phase 1-3 trials, ensuring scientific integrity, and driving regulatory submissions. The Medical Director will collaborate across functions to generate clinical data, engage with external experts, and contribute to global development strategies. The position requires strong medical oversight, real-time safety monitoring, and leadership in oncology research with a focus on innovation and patient impact.

GSK

Hybrid Permanent

Medical Director, Oncology Clinical Development

This role involves leading clinical development activities for oncology assets, including designing and executing phase 1-3 trials, ensuring scientific integrity, and driving regulatory submissions. The Medical Director will collaborate with internal teams and external experts to advance GSK’s oncology pipeline, interpret clinical data, and support lifecycle management strategies. The position requires strong medical expertise in oncology and experience in clinical trial execution and regulatory processes.

GSK PLN 455,250 – PLN 758,750 pa

Hybrid Permanent

Associate Director of Clinical Sciences

Lead clinical sciences strategy and execution for global oncology studies, with responsibility for end-to-end protocol development, clinical data review, and cross-functional collaboration. Focus on immuno-oncology with strong emphasis on regulatory compliance, patient safety, and scientific leadership across clinical development phases. Work within a matrix environment to guide study design, interpretation, and regulatory submissions.

GSK Stevenage, United Kingdom

Senior Medical Director, Oncology Clinical Development - GU

This role involves leading clinical development activities for GSK’s oncology portfolio, with a focus on genitourinary (GU) cancers. The Senior Medical Director will design and execute Phase 1-3 clinical trials, provide medical oversight, interpret clinical data, and engage with external experts and regulatory authorities. The position requires strong leadership in a matrixed environment and deep expertise in oncology drug development.

GSK Stevenage, United Kingdom US$284,250 – US$473,750 pa

Hybrid Permanent

Associate Director of Clinical Sciences

This role involves leading clinical sciences activities in global oncology studies, with responsibility for end-to-end protocol development, clinical data review, and cross-functional collaboration. The individual will shape study design, interpret results, and ensure regulatory compliance across phases of development, with a focus on immuno-oncology. The position requires scientific leadership, engagement with external experts, and contribution to regulatory submissions and clinical strategy.

GSK United States