Latest Medical Services Jobs

Principal Medical Writer

The Principal Medical Writer will lead the creation of high-quality clinical and regulatory documents, working closely with cross-functional teams to ensure scientific rigor and compliance. This role involves strategic planning, project management, and translating complex data into clear narratives, with a focus on regulatory submissions and process improvements.

GSK

On-site Permanent

Principal Medical Writer

The Principal Medical Writer will author and deliver high-quality clinical regulatory documents, lead cross-functional teams in developing clinical dossier documents for global regulatory submissions, and manage complex writing projects. They will interpret complex clinical and statistical information, ensuring compliance with GSK standards and regulatory requirements.

GSK

Hybrid 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

Assistant General Counsel - R&D

Lead legal support for GSK’s R&D Technologies and Translational Sciences teams, advising on collaborations, data governance, and regulatory compliance in drug discovery and development. Provide strategic legal guidance on academic partnerships, data licensing, and sample management while working cross-functionally to mitigate risks and accelerate R&D. Matrix-manage legal colleagues and contribute to policy responses and training to strengthen legal awareness across science teams.

GSK

Hybrid Permanent

Assistant General Counsel - R&D

This role involves providing strategic legal leadership for GSK’s R&D Technologies and Translational Sciences teams, focusing on discovery and translational research platforms. The lawyer will advise on collaborations, data governance, regulatory compliance, and complex agreements with academic and commercial partners, while supporting innovation in biopharma R&D. The position requires close partnership with cross-functional teams and occasional international travel.

GSK

Hybrid Permanent

Statistics Leader / Associate Director – Oncology Statistics

This role involves leading statistical planning and delivery for oncology clinical programs, working closely with cross-functional teams to design robust clinical trials and drive methodological innovation. You will mentor colleagues and contribute to regulatory strategy, using advanced statistical methods and simulations to inform trial design and risk assessment.

GSK

Hybrid Permanent

Statistics Leader / Associate Director – Oncology Statistics

This role involves leading statistical planning and delivery for clinical programs in oncology, working closely with cross-functional teams to design robust clinical trials and contribute to regulatory strategy. The position also focuses on methodological innovation and mentoring colleagues to build statistical capability and quality.

GSK

Hybrid Permanent

Research Pipeline Project Manager

The Research Pipeline Project Manager will lead and coordinate cross-functional pre-clinical research projects, partnering with scientists and clinical teams to advance scientific priorities. Responsibilities include end-to-end planning, risk management, and driving improvements in project delivery processes, with a focus on patient impact and team collaboration.

GSK

Hybrid Permanent

Principal Programmer / Analyst

This role involves leading programming activities for complex clinical studies, ensuring high-quality and timely outputs. You will collaborate with cross-functional teams, mentor junior programmers, and support regulatory interactions, while fostering quality assurance and innovation.

GSK

Hybrid Permanent

Senior Principal Statistician

This role involves leading statistical strategy and innovation in clinical trial design within GSK’s Oncology pipeline. The Senior Principal Statistician will apply advanced methodologies, including Bayesian techniques and simulations, to inform study design, risk assessment, and decision-making across early to late-phase development. Working closely with cross-functional teams, the role emphasizes methodological rigor, high-quality deliverables, and scientific leadership in a collaborative, patient-focused R&D environment.

GSK

Hybrid Permanent

Senior Principal Statistician

This role involves leading statistical strategy and innovation in clinical trial design for oncology drug development. You will apply advanced methodologies including Bayesian techniques, simulations, and risk assessment to support trials from early to late phases. Collaboration with cross-functional teams is central to enabling data-driven decisions in a dynamic R&D environment.

GSK

Hybrid Permanent

Senior Principal Statistician

This role involves leading statistical strategy and innovation in oncology clinical development, designing and analyzing trials from early to late phases using advanced methods like Bayesian statistics. The statistician will collaborate with cross-functional teams, develop analysis plans, and apply simulations to assess trial risk and success probabilities, playing a key technical and strategic role in drug development programs.

GSK

Hybrid Permanent