Latest regulatory affairs Jobs

Global Development Lead, Early Clinical Development, Internal Medicine

The Global Development Lead will drive clinical research for cardiometabolic diseases, creating early clinical development strategies and leading the translation of pre-clinical observations into Phase 1/2 studies. They will work closely with cross-functional teams to ensure medical and scientific excellence, manage clinical trial execution, and engage with regulatory authorities and external collaborators.

Pfizer Sandwich, United Kingdom

On-site Permanent

Senior Manager, Planning and Production Solutions—Label Operations

This role involves leading label design, production, and system operations for clinical trial supplies within a GMP and regulatory-compliant environment. The Senior Manager ensures accurate and timely delivery of packaging and labeling solutions using enterprise systems like PRISYM360 and EMD365, while driving process improvements and digital innovation. Collaboration with internal teams and external vendors is key to supporting global clinical studies and advancing supply chain traceability and efficiency.

Pfizer Sandwich, United Kingdom

Hybrid Permanent

Director, Development Unit CQA Program Lead

Salary Range:£78,400.00 - £145,600.00Job Description Summary#LI-HybridLocation: London (The Westworks), United KingdomRelocation Support: This role is based in London (The Westworks), United Kingdom. Novartis is unable to offer relocation support: please only apply if accessible.Shaping the future of clinical development requires...

Novartis London, United Kingdom

Global Program Safety Team Lead - Neuroscience

This role involves leading medical safety strategy for neuroscience drug development programs at Novartis, managing global cross-functional teams, and ensuring robust benefit-risk evaluation throughout the product lifecycle. The position requires deep expertise in safety signal detection, regulatory submissions, and mentoring safety professionals, with a strong focus on clinical development and lifecycle management. Based in London or remotely, the role plays a key part in shaping global safety standards and driving patient-centric innovation.

Novartis London, United Kingdom £104,790 – £194,610 pa

Hybrid Permanent

Portfolio Innovation Director - Global Clinical Operations

This role involves leading operational innovation within global clinical trials, focusing on integrating AI-driven and technology-enabled solutions to improve trial design, patient access, and efficiency. The director will identify, evaluate, and scale innovations across the portfolio while collaborating with cross-functional teams and external partners. The position emphasizes strategic decision-making, risk assessment, and delivering measurable impact in clinical development.

Novartis London, United Kingdom £83,510 – £155,090 pa

Hybrid Permanent

Portfolio Innovation Director - Global Clinical Operations

The Portfolio Innovation Director will lead the integration of cutting-edge technologies, particularly AI-driven solutions, into global clinical operations at Novartis. This role focuses on identifying, evaluating, and scaling innovations to improve clinical trial design, accelerate recruitment, and enhance patient access. The position requires close collaboration with cross-functional teams and external partners to deliver measurable impact across the clinical portfolio.

Novartis London, United Kingdom

Hybrid Permanent

Investigator Contracts Lead, Sr. Manager

Leads clinical trial site contract negotiations and budget management for global studies, overseeing agreements and amendments with investigator sites. Acts as a key point of contact for complex contracting strategies, collaborates with legal and finance teams, and mentors junior negotiators. Focuses on risk mitigation, timeline adherence, and process improvements in a remote, matrixed environment.

Pfizer London, SW7 2AP, United Kingdom

Remote Permanent

GCP Compliance Manager (GCO)

This role involves leading quality issue management, audit coordination, and inspection readiness for global clinical trials, ensuring compliance with GCP and regulatory standards. The manager will drive self-assessments, conduct risk-based investigations, and provide expert guidance across clinical operations. It’s a high-impact compliance position requiring strong cross-functional influence and operational rigor in a hybrid working environment.

Novartis London, United Kingdom £67,900 – £126,100 pa

Hybrid Permanent

Compliance Engineer (Medical Equipment)

This role involves overseeing legislative compliance and product safety for medical equipment, conducting detailed testing, maintaining compliance databases, and training teams. The position offers opportunities for career progression and in-house training.

Ernest Gordon Recruitment Cheltenham, Gloucestershire, United Kingdom £55,000 pa

On-site Permanent

Test Engineer

This role involves designing and implementing quality test procedures for both software and hardware components of medical devices. Responsibilities include attending design meetings, writing test plans, analyzing opportunities for automated testing, and ensuring compliance with regulatory standards.

Quality Start Walsall, West Midlands (county), United Kingdom £30,000 – £35,000 pa

On-site Permanent

Design Engineer - Medical Devices

Design Engineer - Medical Devices Falmouth, Cornwall | Site-BasedA leading global healthcare company specialising in Women's Health technologies is seeking an Design Engineer to join its growing R&D team in Cornwall. This is an excellent opportunity to work on innovative...

Gold Group Falmouth, Cornwall, United Kingdom £45,000 pa

Test Quality Assurance Engineer

This role involves designing and implementing quality test procedures for both software and hardware in medical device products. Responsibilities include attending design meetings, writing test plans, and ensuring compliance with regulatory standards.

Quality Start Walsall, West Midlands (county), United Kingdom £30,000 – £35,000 pa

On-site Permanent

R&D Consultant - Drug Delivery Device Design - Cambridge

Lead the design and development of innovative drug delivery devices through early-stage concept creation, prototyping, and experimental design. Work within multidisciplinary teams to translate technical challenges into manufacturable medical solutions while advising clients on development pathways and regulatory considerations. Play a hands-on role in R&D leadership and technical mentorship.

Newton Colmore Cambridge, Cambridgeshire, United Kingdom

On-site Permanent

Clinical Quality Assurance - Program Lead (Associate Director)

The Associate Director, Clinical Quality Assurance (QA) will lead quality oversight for clinical trials, ensuring compliance with health authority requirements and patient safety. Responsibilities include implementing quality strategies, monitoring risk management, and supporting governance for quality incidents. The role involves collaboration with key stakeholders and active participation in continuous improvement initiatives.

Novartis London, United Kingdom

Hybrid Permanent

Integrated Insights Business Partner

This role focuses on transforming data into strategic insights to support commercial and access decision-making within specific therapeutic areas. The business partner leads market research, synthesizes internal and external data, and collaborates with cross-functional teams to deliver actionable intelligence. Emphasis is placed on data-driven storytelling, forecasting support, and ensuring consistency across insights functions.

Novartis London, United Kingdom £66,570 – £123,630 pa

On-site Permanent