Latest Drug Discovery Jobs

Clinical Development Medical Director- Hepatology

Lead clinical development strategy and execution for hepatology programs, designing and overseeing translational and clinical studies to advance novel liver disease treatments. Provide medical leadership across cross-functional teams, contribute to regulatory interactions, and drive innovation in drug development. Focus on identifying high-impact targets and delivering differentiated medicines with strong scientific and clinical foundations.

GSK £202,500 – £371,250 pa

Hybrid Permanent

Medical Director Clinical Development- Respiratory

This role involves leading clinical development for respiratory assets within GSK’s Respiratory, Immunology & Inflammation Research Unit. The Medical Director will design and deliver clinical and translational strategies, oversee study execution, ensure patient safety, and contribute to regulatory submissions. Working cross-functionally, they will help shape development plans that align with scientific innovation and patient needs, particularly in pulmonary hypertension and related areas.

GSK £222,750 – £371,250 pa

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 accountability for designing, executing, and interpreting global clinical studies to support regulatory submissions. The individual will act as a key clinical leader, collaborating with cross-functional teams and external stakeholders to shape clinical development plans, trial design, and lifecycle strategies. Expertise in obesity, endocrinology, or chronic weight management is required, along with leadership in managing large-scale clinical programs and regulatory deliverables.

Pfizer £274,500 – £457,500 pa

On-site Permanent

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

This role leads clinical development for Internal Medicine assets within Pfizer's Research & Development division, serving as the primary clinical accountable leader for global drug development programs. The position involves end-to-end responsibility for clinical strategy, trial design, regulatory submissions, and cross-functional team leadership across a complex matrix environment. It also includes engagement with external stakeholders, patient advocacy groups, and oversight of safety and lifecycle planning, with a focus on obesity and related therapeutic areas.

Pfizer £274,500 – £457,500 pa

On-site Permanent

Senior Manager, Trade Operations & Compliance, EMEA

Lead and shape trade compliance strategy across EMEA, ensuring seamless cross-border movement of medicines through robust customs and regulatory frameworks. Drive digital transformation in trade operations using tools like SAP GTS and AI-enabled solutions, while collaborating with cross-functional teams to optimize compliance, reduce costs, and enhance operational agility. Serve as a key liaison with customs authorities and internal stakeholders to maintain regulatory readiness and operational excellence.

Moderna Breckland, IP24 1HF, United Kingdom

Manager, Global Regulatory Science CTA

Lead the end-to-end operational execution of Clinical Trial Applications (CTAs) outside the US, ensuring regulatory compliance and timely submissions across global markets. Serve as the subject matter expert on UK clinical trial regulations, including MHRA requirements and evolving legislation, while leveraging digital tools and AI-enabled technologies to enhance regulatory operations. Collaborate with cross-functional teams and CROs to maintain inspection-ready documentation and drive continuous improvement in regulatory processes.

Moderna Poland

On-site Permanent

SERM Scientific Director

Leads safety evaluation and risk management for GSK's oncology assets in clinical development, providing scientific expertise to assess and communicate safety risks globally. Works cross-functionally to shape safety strategy, support regulatory submissions, and ensure patient protection. Focuses on signal detection, risk assessment, and strategic decision-making in a matrix environment.

GSK £111,750 – £186,250 pa

On-site Permanent

SERM Scientific Director

Provides medical and scientific leadership in the safety evaluation and risk management of ViiV assets during clinical development. Interprets safety data, identifies and escalates safety signals, and delivers evidence-based recommendations to inform benefit-risk decisions. Engages with cross-functional teams, governance bodies, and regulatory authorities to shape the safety profile of specialty medicines and ensure patient safety.

GSK United Kingdom

Hybrid Permanent

Director, Oncology Translational Medicine

Lead the development and execution of biomarker and translational medicine strategies for late-stage oncology programs, integrating cutting-edge technologies to inform clinical decision-making and patient stratification. Collaborate across cross-functional teams to align biomarker strategies with clinical development and regulatory goals. Drive innovation through translational research and real-world data integration to support drug development and life cycle management.

GSK Canterbury, United Kingdom £189,750 – £316,250 pa

SERM Medical Director

Provides medical and scientific leadership in the safety evaluation and risk management of GSK’s oncology assets in clinical development. Interprets safety data, identifies and escalates safety signals, and delivers evidence-based recommendations to support benefit-risk decisions. Engages with global governance, regulatory authorities, and cross-functional teams to shape the safety profile of innovative oncology medicines.

GSK €119,250 – €198,750 pa

On-site Permanent

Director, Oncology Translational Medicine

Leads the development and execution of biomarker and translational medicine strategies for late-stage oncology programs, integrating cutting-edge technologies to identify predictive biomarkers and optimise patient selection. Works within cross-functional clinical teams to embed biomarker-driven decision-making into trial design and development plans. Focuses on validating pharmacodynamic, target engagement, and resistance mechanisms to inform clinical go/no-go decisions and life cycle management.

GSK United States £189,750 – £316,250 pa

Director, Oncology Translational Medicine

Lead the development and execution of biomarker and translational medicine strategies for late-stage oncology assets, integrating cutting-edge technologies to identify predictive biomarkers and optimise clinical decision-making. Collaborate across functions to align biomarker strategies with clinical development plans and support patient segmentation, dose selection, and regulatory strategies. Drive scientific innovation through real-world data, multi-omic analyses, and external partnerships to advance GSK’s oncology pipeline.

GSK US$189,750 – US$316,250 pa

SERM Scientific Director

This role involves leading pharmacovigilance and risk management strategies for GSK's global assets, with a focus on safety evaluation and benefit-risk management across clinical development and post-marketing settings. The position requires expert analysis of clinical and safety data, leadership in cross-functional governance teams, and strategic input into regulatory submissions and risk mitigation. It plays a critical part in ensuring patient safety and regulatory compliance within immunology and other therapeutic areas.

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 immunology. The Scientific Director will evaluate safety data, lead cross-functional teams, and ensure compliance in clinical development and post-marketing settings. The position requires deep expertise in safety evaluation, signal detection, and international regulatory standards.

GSK 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 immunology and other therapeutic areas. The Scientific Director will oversee safety governance, lead cross-functional teams, and ensure compliance with global regulations. They will analyze clinical data, manage safety issues, and contribute to regulatory submissions and long-term clinical strategy.

GSK US$169,950 – US$283,250 pa

On-site Permanent