Latest regulatory affairs Jobs

Senior Regulatory Managers

This role involves leading Chemistry, Manufacturing and Controls (CMC) regulatory activities across development, registration, and early lifecycle stages. You will work with cross-functional teams, provide regulatory advice, and support inspections and quality events. The position offers opportunities for growth through complex regulatory work and direct impact on patient health.

GSK

Hybrid Permanent

Senior Regulatory Managers

This role involves leading Chemistry, Manufacturing and Controls (CMC) regulatory activities across development, registration, and early lifecycle stages. You will work with cross-functional teams, provide regulatory advice, and manage interactions with regulatory authorities, ensuring compliance and supply continuity.

GSK

Hybrid Permanent

Global Labelling Manager, Content

The Global Labelling Manager, Content will lead the development and maintenance of high-quality global labelling documents for pharmaceutical products. Key responsibilities include organising cross-functional discussions, conducting research on competitor labels and regulatory guidance, and ensuring compliance with global standards across the product lifecycle.

Novartis London, United Kingdom

Hybrid Permanent

Global Labelling Associate Director, Content

This role involves developing and maintaining global labelling strategies and core documents for pharmaceutical products. You will lead cross-functional discussions, present labelling proposals, and ensure compliance with regulatory requirements across different markets.

Novartis London, United Kingdom

Hybrid Permanent

Director, Medical Insights

The Director, Medical Insights role involves shaping and implementing Medical Insights processes, collaborating with various stakeholders to generate actionable insights, and embedding these insights into medical decision-making. The role focuses on leveraging advanced analytics and AI to translate complex medical data into strategic decisions, ensuring consistency and value across Pfizer’s medical portfolio.

Pfizer

On-site Permanent

Director, Medical Insights

The Director, Medical Insights role at Pfizer involves shaping and implementing Medical Insights processes, collaborating with various stakeholders, and leveraging advanced analytics and AI to translate complex medical data into actionable insights. The role focuses on embedding these insights into medical decision-making and strategic discussions, ensuring they are relevant and impactful across Pfizer’s portfolio of medicines.

Pfizer

Remote Permanent

Associate Director, CMC Regulatory Science, International

This role involves developing and implementing CMC regulatory strategies for global submissions, providing guidance on regulatory CMC aspects, and ensuring compliance with health authority guidelines. The candidate will support multiple programs in various therapeutic areas, including vaccines, oncology, and rare diseases, and contribute to the development of regulatory processes and procedures.

Moderna

On-site Permanent

Associate Director, Global Regulatory Science, CMC

Lead global CMC regulatory strategy for mRNA medicines, guiding international submissions and ensuring compliance with health authority requirements. Collaborate with manufacturing and quality teams to support product development across vaccines, oncology, and rare diseases. Develop and maintain regulatory documentation in CTD format, while driving process improvements and change control assessments.

Moderna

Hybrid Permanent

Sr. Scientist / APS, Data Compliance & Governance Management

This role focuses on enabling compliant cross-border data transfers for AstraZeneca’s Beijing AI Center by preparing scientific data for review, ensuring regulatory alignment, and streamlining processes. The candidate will triage data requests, assess compliance with regulations like DOJ EO 14117, trace data provenance, curate datasets, and coordinate with global stakeholders across R&D, privacy, and legal teams. The position bridges scientific data operations and governance to support AI-driven drug discovery while building scalable processes for future data sharing.

AstraZeneca Cambridge, United Kingdom

Hybrid Permanent

Senior Clinical Trial Case Manager

This role involves leading cross-functional teams in reviewing safety data, mentoring junior staff, and ensuring compliance with GxP guidelines and international regulations. The position also focuses on managing pharmacovigilance procedures, conducting impact assessments of new legislation, and supporting regulatory inspections and audits.

CSL

On-site Permanent

Director Biostatistics

The Director of Biostatistics leads the statistical aspects of clinical development programs, ensuring robust study design, data analysis, and regulatory submissions. They collaborate closely with cross-functional teams and regulatory authorities to drive the success of clinical trials and therapeutic programs.

CSL

Hybrid Permanent

Director, Project Toxicologist – Oncology Targeted Delivery Safety Science

This role involves leading toxicology strategy for oncology drug development, focusing on novel targeted therapies such as Radio Conjugates and Antibody Drug Conjugates (ADCs). The Director will design regulatory and investigative studies, integrate safety data using advanced in vitro, in silico, and in vivo methods, and guide cross-functional teams from discovery through to clinical translation. Emphasis is placed on innovation in safety science, including the use of emerging technologies like organ-on-chip and omics.

AstraZeneca Cambridge, United Kingdom

On-site Permanent

Associate Director/Director of Statistical Programming

This role involves leading statistical programming activities across clinical programs, ensuring the development and quality control of tables, listings, figures, and analysis datasets. You will oversee external vendors, develop standards and innovative technologies, and support data-driven decision-making in drug discovery.

Recursion United Kingdom £200,600 – £260,200 pa

Remote Permanent

Buyer - Pharmaceuticals

This role involves managing procurement activities, supplier relationships, and quality management within a regulated pharmaceutical manufacturing environment. You will work closely with the Manufacturing, Quality, and Operations teams to ensure effective sourcing and compliance with GMP standards.

Cranleigh Scientific Ditton, Kent, ME20 6AE, United Kingdom £22,800 – £28,800 pa

Hybrid Flexible

QA/ Validation Supervisor, Pharmaceutical

This role involves leading a small QA team, ensuring compliance with regulatory standards, and overseeing quality systems and validation activities. Responsibilities include report writing, internal and external audits, and driving continuous improvement initiatives.

NMS Recruit Ltd t/a Russell Taylor Group Walkden, Manchester, M28 3DR, United Kingdom £40,000 – £45,000 pa

On-site Permanent