Latest Medical Affairs Partner - Nephrology & R Jobs

Senior Manager - CMC Regulatory Affairs Biopharm Development Projects

This role involves leading CMC regulatory activities for GSK's investigational, late development, and early commercial products. Responsibilities include driving CMC strategy, preparing regulatory documents, managing project activities, and mentoring staff. The position requires a strong understanding of regulatory requirements and the ability to communicate complex issues across departments and with external agencies.

GSK

On-site Permanent

Director, CMC Regulatory Affairs

Leads global CMC regulatory strategy for small molecule medicines, shaping development and approval pathways across international markets. Works at the intersection of R&D, supply, quality, and commercial functions to ensure regulatory compliance and uninterrupted patient access. Focuses on solving complex regulatory challenges, mentoring talent, and improving processes to support long-term product success.

GSK East Hertfordshire, United Kingdom

Hybrid Permanent

SERM Scientific Director

The SERM Scientific Director role involves leading pharmacovigilance and risk management planning, developing safety strategies, and ensuring the scientific soundness of data reviews. The position requires expertise in evaluating safety risks, managing cross-functional teams, and communicating safety issues to senior management.

GSK

On-site Permanent

SERM Scientific Director, Oncology

The SERM Scientific Director role involves leading pharmacovigilance and risk management strategies for clinical development and post-marketing products. Responsibilities include evaluating safety data, managing safety concerns, and supporting regulatory activities. The role operates in a global, cross-functional environment and may include mentoring responsibilities.

GSK United Kingdom

Hybrid Permanent

VP, Medicine Development Leader - Respiratory

This role leads the global development of a respiratory medicine from clinical proof of concept through to approval, serving as the strategic and operational leader of a cross-functional matrix team. The VP Medicine Development Leader defines the asset’s vision, drives evidence-based decision-making, and ensures alignment across R&D, manufacturing, regulatory, and commercial functions to deliver differentiated medicines for patients. The position involves shaping development plans, managing budgets, engaging with regulators, and supporting lifecycle strategies while representing the asset to senior leadership and external stakeholders.

GSK Stevenage, United Kingdom US$309,750 – US$516,250 pa

Hybrid Permanent

VP, Medicine Development Leader - Respiratory

This role leads the global development of a respiratory medicine from clinical proof of concept through to regulatory approval, serving as the primary accountable leader across a matrixed cross-functional team. The VP will define strategic direction, oversee clinical and regulatory planning, manage budgets, and ensure alignment with GSK’s broader R&D and commercial objectives. The position involves high-level stakeholder engagement, lifecycle planning, and external representation to regulators and advisory bodies.

GSK United States £309,750 – £516,250 pa

Hybrid Permanent

VP, Medicine Development Leader - Respiratory

Lead the global development of a respiratory medicine from clinical proof of concept through to first-market approval, serving as the single point of accountability. You will build and lead a cross-functional matrix team, define strategic direction, and ensure alignment with GSK’s R&D and commercial strategies. The role involves shaping lifecycle plans, making evidence-based go/no-go decisions, and engaging with regulators and senior leadership to deliver patient-focused medical solutions.

GSK US$309,750 – US$516,250 pa

Hybrid Permanent

VP, Medicine Development Leader - Respiratory

Leads global development of a respiratory medicine from clinical proof of concept to approval, aligning cross-functional teams across R&D, manufacturing, and commercial functions. Defines strategic vision, manages development plans, regulatory submissions, and lifecycle strategy while ensuring patient-focused innovation and compliance. Acts as primary point of accountability and spokesperson to senior leadership and external stakeholders.

GSK US$309,750 – US$516,250 pa

Hybrid Permanent

VP, Medicine Development Leader - Respiratory

This role leads the global development of a respiratory medicine from proof of concept through to approval, serving as the primary accountable leader across a cross-functional matrix team. The VP will define strategic direction, oversee clinical and regulatory execution, and align development with GSK’s broader R&D and commercial strategy, while engaging with senior leadership and external stakeholders to advance patient-focused innovation.

GSK US$309,750 – US$516,250 pa

Hybrid Permanent

VP, Medicine Development Leader - Respiratory

Leads global development of a respiratory medicine from clinical proof of concept through approval, serving as the primary accountable leader across a cross-functional matrix team. Defines strategic vision, drives evidence generation, lifecycle planning, and regulatory strategy while coordinating input from R&D, manufacturing, commercial, and regulatory stakeholders to deliver patient-focused therapies.

GSK US$309,750 – US$516,250 pa

Hybrid Permanent

Senior Scientist ETCT

The Senior Scientist will work within the ETCT Biology Unit, contributing to pre-clinical and early clinical biologics programs. Responsibilities include designing and executing experiments, providing input on pharmacokinetics and non-clinical safety, and mentoring junior scientists.

GSK Stevenage, United Kingdom

Hybrid Permanent

Senior Director Translational Data Sciences

This role involves developing and executing a translational data strategy that bridges the gap between disease biology and clinical outcomes. The Senior Director will lead a team in integrating multi-omics data with AI-driven analytics, forming strategic partnerships, and ensuring clinical relevance in all analytical platforms.

GSK Stevenage, United Kingdom

On-site Permanent

Statistics Director, Oncology

This role involves leading statistical strategies for key oncology programs, designing robust clinical trials, and mentoring statisticians. The position emphasizes innovation, regulatory interactions, and cross-functional collaboration to advance the development of new cancer therapies.

GSK Stevenage, United Kingdom

On-site Permanent

Process Safety Engineer

This role involves providing expert process safety leadership at GSK’s Barnard Castle manufacturing site, ensuring compliance with EHS regulations and delivering process safety improvements. The engineer will lead hazard assessments, support incident investigations, and drive safe working practices across production operations, with a strong focus on regulatory standards like DSEAR and CDM. The position plays a key part in maintaining safety integrity within a high-value, regulated pharmaceutical environment.

GSK Barnard Castle, United Kingdom

On-site Permanent

Device Technologist - 12 Month Secondment

The Device and Packaging Technologist provides technical support for device assembly and packaging activities, including new product introduction, change control, and continuous improvement. The role involves collaborating with site teams, central technology functions, and external suppliers to ensure compliant and efficient solutions throughout the product lifecycle.

GSK Barnard Castle, United Kingdom

On-site Contract