Latest Professional Services Jobs

MSAT Molecule Steward

This role involves providing end-to-end technical leadership for a pharmaceutical product throughout its lifecycle, from development to commercial manufacturing. The Molecule Steward ensures product quality, robustness, and manufacturability by leading technical strategy, process optimization, and regulatory compliance across global supply chain teams. The position requires deep scientific expertise, cross-functional collaboration, and leadership in resolving complex technical challenges in a regulated environment.

GSK €103,500 – €172,500 pa

Hybrid Permanent

Quality Manager (on Shift)

The Quality Manager on Shift ensures compliance with GMP and regulatory requirements during manufacturing and non-manufacturing activities. Key responsibilities include monitoring quality systems, investigating deviations, and supporting product release. The role involves working in a 24/5 shift pattern, including weekends, and promoting team collaboration and continuous improvement.

GSK East Hertfordshire, United Kingdom

On-site Permanent Shift-work

Disease Area Lead - Hepatology, Renal and Cardiovascular diseases

This role leads clinical operations strategy and delivery for GSK's Hepatology, Renal, and Cardiovascular disease portfolio, overseeing end-to-end development from early phase through post-marketing. The leader will manage a matrix team, drive operational excellence, embed data-driven decision-making, and align with enterprise goals to ensure high-quality, efficient clinical delivery across global programs.

GSK US$242,550 – US$404,250 pa

On-site Permanent

Product Manager - Regulatory Vault

Are you passionate about making impactful contributions to the world of medicines and vaccines? GlaxoSmithKline (GSK) invites you to join our dynamic R&D Digital and Tech Team as a Product Manager - Regulatory Vault. In this pivotal role, you will...

GSK United Kingdom

Disease Area Lead - Hepatology, Renal and Cardiovascular diseases

Leads clinical operations strategy and delivery for GSK's Hepatology, Renal, and Cardiovascular disease portfolio, overseeing end-to-end development from early phase through phase IV. Responsible for shaping operational direction, managing cross-functional teams, driving data-led decision-making, and ensuring alignment with enterprise goals. Focuses on innovation, risk management, and talent development within a global R&D environment.

GSK US$242,550 – US$404,250 pa

On-site Permanent

Senior Director, Head of Global Medical Governance, ViiV Healthcare

This role involves leading the global medical governance system at ViiV Healthcare, ensuring compliance and ethical standards across all medical activities. Responsibilities include developing and maintaining governance policies, advocating for medical governance, and collaborating with regional teams to embed best practices.

GSK United Kingdom

On-site Permanent

Senior Director, Head of Global Medical Governance, ViiV Healthcare

This role involves leading the global medical governance system at ViiV Healthcare, ensuring ethical and compliant medical practices across the organization. Responsibilities include developing and maintaining governance policies, advocating for medical governance, and collaborating with regional and local teams to embed robust practices.

GSK

On-site Permanent

Senior Global Medical Director Oncology

This role involves leading the global medical strategy for a lung cancer asset, working with cross-functional teams to translate scientific insights into practical patient impact. Responsibilities include chairing global medical teams, managing external partnerships, and ensuring scientific quality and compliance.

GSK US$241,500 – US$402,500 pa

On-site Permanent

Senior Global Medical Director Oncology

This role involves leading the global medical strategy for a lung cancer asset, working with cross-functional teams to translate scientific insights into practical patient impact. Responsibilities include chairing a global medical team, managing external partnerships, and ensuring scientific quality and compliance.

GSK US$241,500 – US$402,500 pa

Remote Permanent

Statistics Director, Oncology

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

GSK United Kingdom

On-site Permanent

Statistics Director, Oncology

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

GSK

On-site Permanent

Clinical Programmer/Analyst

The Clinical Programmer/Analyst designs, builds, and reviews programming solutions to transform clinical and real-world data into reliable results for analysis and reporting. Working closely with statisticians and cross-functional teams, the role involves developing validated datasets, tables, listings, and figures in compliance with regulatory standards such as SDTM, ADaM, and TFL. The position supports agile delivery within a hybrid work environment and emphasizes code quality, regulatory adherence, and innovation in data programming practices.

GSK United Kingdom

Hybrid Permanent

NIS P&D Study Delivery Lead, Associate Director

The NIS P&D Study Delivery Lead, Associate Director, is responsible for leading the full lifecycle of clinical studies and trials within the Non-Interventional Study (NIS) portfolio. This includes designing, executing, and reporting complex regulatory commitment studies, managing team members, and ensuring compliance with regulatory guidelines. The role also involves leading operational decision-making, risk management, and driving innovation in study delivery through new technologies.

GSK £87,000 pa

Permanent

Director, CMC Regulatory Affairs

Leads global CMC regulatory strategy for small molecule medicines, working across R&D, supply, quality, and commercial functions to ensure regulatory compliance and uninterrupted patient supply. Provides strategic direction on regulatory submissions, mentors regulatory staff, and engages with global authorities. Focuses on solving complex regulatory challenges while aligning with business objectives and patient impact.

GSK

Hybrid Permanent

Assistant General Counsel - R&D

Lead legal support for GSK’s R&D discovery and translational platforms, advising on collaborations, data governance, regulatory compliance, and risk management. Partner with scientific and business leaders to enable technology-driven drug discovery and development, draft complex agreements, and provide strategic legal guidance in a global, science-led environment.

GSK United Kingdom

Hybrid Permanent