Latest Innovation Jobs

Regional Medical Advisor

The EU and International Regional Medical Advisor role involves representing the business voice, leveraging medical platforms, and aligning medical affairs processes across the EU and International regions. Key responsibilities include supporting transversal business prioritization, improving communication with local operating companies, and assisting with data generation processes and real-world evidence studies.

GSK

On-site Permanent

Regional Medical Advisor

The EU and International Regional Medical Advisor role involves representing the business voice, leading the implementation of Medical Affairs processes, and supporting transversal business prioritization. You will work closely with Local Operating Companies to ensure effective communication, conduct impact assessments, and support data generation processes, including Investigator-Sponsored Studies and Real World Evidence initiatives.

GSK

On-site Permanent

Support Engineer, London

As a Support Engineer, you will provide technical support, troubleshoot complex issues, and develop automation tools to improve efficiency. You will collaborate with other teams to resolve technical issues, manage 3rd party integrations, and contribute to the onboarding of new employees. This role is crucial for shaping the support strategy and driving innovation through automation.

Isomorphic Labs United Kingdom

Hybrid Permanent

PKPD Modelling Lead, London

Isomorphic Labs is applying frontier AI to help unlock deeper scientific insights, faster breakthroughs, and life-changing medicines with an ambition to solve all disease.The future is coming. A future enabled and enriched by the incredible power of machine learning. A...

Isomorphic Labs London, United Kingdom

Global Development Lead, Internal Medicine, Sr. Director (MD)

The Global Development Lead (GDL) is responsible for leading the clinical development of assigned assets in Internal Medicine. This involves designing, executing, and interpreting clinical studies, creating development plans, and collaborating with cross-functional teams to ensure regulatory submissions and product approvals globally.

Pfizer

On-site Permanent

Global Development Lead, Internal Medicine, Sr. Director (MD)

The Global Development Lead (GDL) is responsible for leading the clinical development of assigned assets in Internal Medicine. This role involves designing and executing clinical trials, creating development plans, and collaborating with cross-functional teams to ensure regulatory submissions and product approvals globally. The GDL also provides expert input on trial design, regulatory activities, and external stakeholder engagement.

Pfizer

On-site Permanent

Field Service Engineer, Medical Diagnostic Systems

Field Service Engineer, Medical Diagnostic SystemsOverall Earnings £60,000+Basic Salary Up To £52,000OvertimeOn Call Allowance10% BonusCompany Car (Electric Or Hybrid)PensionHealthcareLife InsurancePhone, LaptopHolidays** The role will involve working one weekend in four (during this week you will receive two alternative days off...

TRS Consulting Sutton, United Kingdom

Field Service Engineer, Medical Diagnostic Systems

Field Service Engineer, Medical Diagnostic SystemsOverall Earnings £60,000+Basic Salary Up To £52,000OvertimeOn Call Allowance10% BonusCompany Car (Electric Or Hybrid)PensionHealthcareLife InsurancePhone, LaptopHolidays** The role will involve working one weekend in four (during this week you will receive two alternative days off...

TRS Consulting Croydon, United Kingdom

Sr. Data Platform Engineer - Computer System Validator

As a Senior Data Platform Engineer, you will build, scale, and operate a validated data platform with petabyte-scale data, ensuring data integrity and traceability in a GxP-compliant environment. You will collaborate with biologists, chemists, and data scientists to make Recursion’s vast datasets discoverable and queryable, supporting the company’s mission to advance drug discovery through technology and biology.

Recursion United Kingdom £142,500 – £220,500 pa

Hybrid Permanent

Director, Neuroscience (In Vitro Cellular Biology)

This role involves leading the development and application of human iPSC-derived cellular models for neurodegenerative disease drug discovery. You will design and oversee cellular and molecular assays, collaborate with cross-functional teams, and mentor scientists to advance therapeutic discovery.

Recursion United Kingdom £198,000 – £237,600 pa

Hybrid Permanent

Global Safety Lead - Formulation Safety

Located within CSLB’s GSPV department, the Director, Global Safety Lead, Formulation Safety provide expertise on all aspects of –clinical safety throughout the entire lifecycle of a product with special emphasis on ongoing evaluation of safety information during clinical development and...

CSL

Global Safety Lead - Formulation Safety

Located within CSLB’s GSPV department, the Director, Global Safety Lead, Formulation Safety provide expertise on all aspects of –clinical safety throughout the entire lifecycle of a product with special emphasis on ongoing evaluation of safety information during clinical development and...

CSL

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 work closely with manufacturing and quality teams.

Moderna London, United Kingdom

On-site Permanent

Clinical Data Analyst – Evinova

The Clinical Data Analyst role involves managing and optimizing clinical trial data, collaborating with cross-functional teams, and contributing to the development of data products. Responsibilities include data management, standards validation, pipeline configuration, troubleshooting, and continuous process improvement.

AstraZeneca London, United Kingdom

On-site Permanent

Associate Director, CMC Regulatory Affairs, International

This role involves developing and implementing CMC regulatory strategies for international submissions, providing guidance on regulatory CMC aspects, and leading discussions with health authorities. The candidate will also support the creation of CMC submission templates and offer interpretations of regulatory guidance documents, ensuring compliance and efficient delivery of high-quality regulatory documentation.

Moderna London, United Kingdom

On-site Permanent