Latest Healthcare Jobs

Clinical Sciences Project Manager

This role involves managing and refining processes for investigator-sponsored research studies, supporting the Global Collaborative Studies Group in evidence generation, and leading the Request for Proposal study process. The candidate will work cross-functionally with various teams to ensure timely and compliant delivery of studies and contribute to the mission of advancing HIV research and treatment.

GSK United Kingdom

On-site Permanent

Clinical Sciences Project Manager

This role involves developing and refining processes, risk management strategies, and other activities essential to the success of the Global Collaborative Studies Group (CSG) at ViiV Healthcare. You will lead the Request for Proposal study process, manage study-related activities, and work cross-functionally with various teams to ensure timely and compliant delivery of supported studies.

GSK

On-site Permanent

Labelling Strategy and Development, Oncology Team Lead

Leads a global team responsible for developing and managing oncology product labeling strategies across the R&D lifecycle. This role ensures regulatory compliance, collaborates with cross-functional stakeholders, and shapes patient-focused labeling standards while advising senior leadership and engaging with regulatory authorities to drive innovation in labeling practices.

GSK United States

Hybrid Permanent

Labelling Strategy and Development, Oncology Team Lead

Lead a global team responsible for developing and managing oncology product labelling strategies across the R&D lifecycle. This role involves shaping compliant, patient-focused labels, advising senior stakeholders, and engaging with regulatory authorities to drive innovative approaches. The position requires strong leadership, regulatory expertise, and cross-functional collaboration within a hybrid working model.

GSK

Hybrid Permanent

Labelling Strategy and Development, Oncology Team Lead

This role involves leading a global labelling team for oncology products, shaping clear and compliant product labels that support patient care and regulatory success. The position requires strategic oversight of labelling development from early stages through lifecycle management, working closely with cross-functional teams and regulatory authorities to drive innovative, patient-focused solutions.

GSK

Hybrid Permanent

Labelling Strategy and Development, Oncology Team Lead

Leads a global team responsible for developing and managing oncology product labelling across the drug development lifecycle. This role shapes regulatory-compliant, patient-focused labels by collaborating with cross-functional stakeholders in R&D, Regulatory, Safety, and Commercial. It involves strategic decision-making, engagement with health authorities, and driving innovation in labelling standards to support GSK’s oncology portfolio.

GSK

Hybrid Permanent

Medical Director, Oncology Clinical Development

The Medical Director, Oncology Clinical Development will lead clinical research activities for GSK’s oncology portfolio, collaborating with various stakeholders to develop and execute phase 1-3 clinical trials. Key responsibilities include protocol development, medical monitoring, safety data review, and strategic partnerships with key external experts.

GSK Stevenage, United Kingdom

Hybrid Permanent

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

This role involves planning and executing studies to generate robust health outcomes data for GSK's oncology products. The Director will collaborate with internal and external stakeholders to ensure evidence supports market positioning, reimbursement, and patient access. Key responsibilities include managing study timelines, ensuring deliverable quality, and translating customer needs into study concepts.

GSK United States

On-site Permanent

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

This role involves planning and executing real-world evidence studies to support the launch and market positioning of GSK's oncology drugs. The Director will collaborate with internal and external stakeholders to ensure the generation of high-quality, scientifically credible evidence that meets regulatory and payer requirements.

GSK

On-site Permanent

Director, Global Strategic Insights – Oncology

This role involves leading the generation of strategic insights to shape the global product strategy for a key oncology brand in GSK's ADC portfolio. Responsibilities include driving commercial forecasts, conducting market research, and collaborating with cross-functional teams to ensure insights are integrated into business decisions and investment planning.

GSK United States

On-site Permanent

Director, Global Strategic Insights – Oncology

This role involves leading the generation of strategic insights for a key oncology brand within GSK's ADC portfolio. Responsibilities include shaping commercial forecasts, conducting global market research, and partnering with cross-functional teams to drive business strategy and competitive intelligence.

GSK

On-site Permanent

Director, Global Strategic Insights – Oncology

The Director, Global Strategic Insights – Oncology role involves leading the generation of strategic insights to shape the global product strategy for a key oncology brand. Responsibilities include driving commercial forecasts, commissioning market research, and partnering with cross-functional teams to ensure insights are integrated into business decisions. The role requires a strong background in pharmaceuticals, oncology commercialization, and market research, with a focus on leveraging data to influence business strategy.

GSK

On-site Permanent

SERM Scientific Director

This role involves leading pharmacovigilance and risk management strategies for GSK’s global assets, with a focus on safety evaluation in clinical development and post-marketing settings. The Scientific Director will lead cross-functional teams, drive safety governance, and ensure regulatory compliance across international markets. The position requires deep expertise in drug safety, signal detection, and benefit-risk assessment to protect patient safety and support regulatory submissions.

GSK United States US$169,950 – US$283,250 pa

On-site Permanent

SERM Scientific Director

This role involves leading pharmacovigilance and risk management strategies for GSK's global assets, with a focus on safety evaluation in clinical development and post-marketing settings. The Scientific Director provides expert scientific input into safety governance, drives cross-functional teams, and ensures compliance with global regulatory standards. They play a key role in signal detection, safety surveillance, and shaping long-term clinical strategies to protect patient safety.

GSK US$169,950 – US$283,250 pa

On-site Permanent

SERM Scientific Director

This role involves leading pharmacovigilance and risk management for GSK's global assets, ensuring scientifically sound review and interpretation of safety data. The director will develop and execute safety strategies, manage safety governance, and lead cross-functional teams to address product safety issues and ensure patient safety globally.

GSK

On-site Permanent