Latest Life Sciences Jobs

SPQS Data Steward

This role involves leading the implementation of data stewardship frameworks for Structured Product Quality Submissions (SPQS) within a regulated pharmaceutical environment. The individual will establish metadata standards, controlled vocabularies, and data quality controls across R&D, supply chain, regulatory, and quality functions. They will coordinate cross-functional data governance, ensure compliance, and support digital transformation through structured regulatory submissions.

GSK €83,250 – €138,750 pa

SPQS Data Steward

Lead the implementation of data stewardship and governance frameworks for Structured Product Quality Submissions (SPQS) across global regulatory and manufacturing domains. Translate domain decisions into metadata standards, controlled vocabularies, and data quality controls while collaborating with R&D, Supply Chain, Regulatory, and Quality teams. Drive digital transformation by embedding data governance into business processes and digital solutions to support future regulatory submissions.

GSK €83,250 – €138,750 pa

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

Leads clinical development for assigned assets in Internal Medicine, driving global clinical strategy, trial design, execution, and regulatory submissions. Serves as primary clinical accountability, collaborating with cross-functional teams and external stakeholders to advance drug development programs from concept through approval, with potential focus on obesity-related therapeutics.

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, with accountability for designing and executing global clinical development plans. The position involves leading cross-functional teams, driving regulatory submissions, and serving as a therapeutic expert in obesity and related areas. It requires collaboration with internal and external stakeholders, including regulatory authorities and advisory boards, to shape clinical strategy and ensure successful drug development.

Pfizer

On-site Permanent

Sr Director/Director and Team Lead, Global Regulatory Strategy - LCM

Leads the development and execution of global regulatory lifecycle strategies for assigned assets, ensuring alignment with GSK's medicine development plans and regulatory requirements across key markets. Acts as the primary regulatory point of contact on cross-functional teams, drives innovation in regulatory approaches, and provides strategic input to business development and crisis management. Directly manages a team and collaborates with senior leaders and health authorities worldwide.

GSK United Kingdom

Hybrid Permanent

Platform Equipment Lead (Metrology)

This role involves leading metrology and calibration systems at GSK’s Ware site, ensuring compliance with GMP and engineering standards. You’ll oversee calibration services, lead technical investigations, improve measurement systems, and support capital projects using data-driven insights. The position offers technical leadership, cross-functional collaboration, and strategic impact within a regulated pharmaceutical manufacturing environment.

GSK East Hertfordshire, United Kingdom

Clinical Programmer/Analyst

The role involves developing, testing, and validating programming code to transform and analyze clinical and real-world data for use in regulatory submissions and scientific reporting. You'll collaborate with statisticians and data scientists to ensure outputs meet CDISC standards and regulatory requirements, while contributing to programming best practices within an agile environment. The position emphasizes code quality, compliance with GxP and ICH guidelines, and the use of modern tools and methodologies in a hybrid work setting.

GSK Stevenage, United Kingdom

Hybrid Permanent

Quality Governance & Partnership Senior Specialist

This role involves managing quality governance systems for raw materials and suppliers at GSK’s manufacturing site. The specialist ensures compliance with pharmaceutical regulations, oversees supplier quality workflows, handles change controls and audits, and maintains documentation for material specifications and supplier agreements. The position plays a key role in maintaining supply chain integrity and regulatory compliance within a highly regulated biopharma environment.

GSK Barnard Castle, United Kingdom

Clinical Programmer/Analyst

The Clinical Programmer/Analyst designs, builds, and reviews programming solutions to transform clinical and real-world data into reliable, compliant outputs. Working closely with statisticians and data scientists, the role involves developing code for data transformation, analysis, and reporting in line with CDISC standards (SDTM, ADaM) and regulatory requirements. The position supports agile delivery of high-quality datasets, tables, listings, and figures while promoting programming best practices and innovation within a collaborative, cross-functional environment.

GSK United Kingdom

Hybrid Permanent

Sterility Assurance Senior Expert

This role involves leading sterility assurance projects and overseeing facility compliance with regulatory standards in a pharmaceutical manufacturing environment. The individual will drive contamination control strategies, ensure adherence to cGMP and industry regulations, and act as the primary point of contact during audits. Collaboration with operations and quality teams is essential to integrate sterility assurance into manufacturing processes and support continuous improvement.

GSK Barnard Castle, United Kingdom

Clinical Development Medical Director- Hepatology

Lead clinical development for hepatology assets, designing and executing translational and clinical studies to advance novel liver disease treatments. Provide medical oversight, shape development strategies, and collaborate across functions to deliver innovative medicines. Engage with regulators and external experts to drive proof-of-concept and lifecycle expansion opportunities.

GSK Stevenage, United Kingdom US$202,500 – US$371,250 pa

Hybrid Permanent

Clinical Development Medical Director- Hepatology

Lead clinical development strategy and execution for hepatology assets within GSK’s Respiratory, Immunology & Inflammation Research Unit. Provide medical oversight across translational and clinical studies, design development plans and protocols, and guide decision-making for early-phase programs. Work cross-functionally to advance novel liver disease treatments from discovery through clinical proof of concept, leveraging biomarker and real-world data to inform development.

GSK United Kingdom US$202,500 – US$337,500 pa

Hybrid Permanent

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

Clinical Development Medical Director- Hepatology

Lead clinical development for hepatology assets within GSK’s Respiratory, Immunology & Inflammation Research Unit, driving translational research and early-phase clinical trials to validate novel liver disease targets. Provide medical oversight, design clinical development plans, and collaborate cross-functionally to advance innovative therapies from discovery through development. Work in a hybrid model with significant scientific leadership and regulatory engagement responsibilities.

GSK

VP, Medicine Development Leader - Specialty Product Development

This role leads the global development of a medicine from clinical proof of concept to first-market approval, serving as the single point of accountability within GSK's matrixed R&D environment. The VP Medicine Development Leader will build and lead a cross-functional team, define strategic development plans, and ensure alignment with regulatory, commercial, and manufacturing stakeholders. The position emphasizes evidence-based decision-making, lifecycle planning, and patient-focused development across multiple indications.

GSK Stevenage, United Kingdom £242,250 – £403,750 pa