Future Tech Jobs
Future Tech Jobs
Latest UK roles, updated daily.
ROLE SUMMARYThe Medical Affairs AI Lead is the strategic architect and technical product owner for AI transformation across HQ Medical Affairs and Field Medical. This role defines the AI vision and roadmap, identifies and prioritizes high-impact use cases, builds rapid...
This role involves leading the development and delivery of an intelligent content operating system called AMP, which connects how marketers plan, create, review, and measure content. The Product Lead will define the product vision, strategy, and roadmap, working closely with global stakeholders to ensure alignment and drive measurable outcomes in productivity, quality, and compliance.
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...
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...
This role involves leading the development and delivery of the AMP (Agentic Marketing Platform) – an intelligent content operating system that connects how marketers plan, create, review, and measure content. The Product Lead will define the product vision, roadmap, and success metrics, manage a team of product owners, and collaborate with global stakeholders to ensure alignment and adoption across the marketing and technology ecosystem.
This role involves overseeing medical and scientific aspects of clinical trials in Internal Medicine, ensuring data integrity and quality. Responsibilities include medical monitoring, safety data review, protocol development, and collaboration with internal and external stakeholders.
This role involves overseeing medical and scientific aspects of clinical trials in Internal Medicine, ensuring data integrity and quality. Responsibilities include medical monitoring, safety data review, protocol development, and collaboration with internal and external stakeholders. The position also involves mentoring others and contributing to the overall clinical strategy.
This role involves overseeing medical and scientific aspects of clinical trials in Internal Medicine, ensuring data integrity and quality. Responsibilities include medical monitoring, safety data review, protocol development, and providing clinical support to study teams and investigators.
This role involves overseeing the medical and scientific aspects of clinical trials in Internal Medicine, ensuring data integrity and quality. Responsibilities include medical monitoring, safety data review, protocol development, and providing clinical support to study teams and investigators.
This role involves overseeing the medical and scientific aspects of clinical trials in Internal Medicine, ensuring data integrity and quality. Responsibilities include medical monitoring, safety data review, protocol development, and providing clinical support to study teams and investigators.
This role involves overseeing medical and scientific aspects of clinical trials in Internal Medicine, ensuring data integrity and quality. Responsibilities include medical monitoring, safety data review, protocol development, and providing clinical support to study teams and external stakeholders.
This role involves overseeing the medical and scientific aspects of clinical trials in Internal Medicine, ensuring data integrity and quality. Responsibilities include medical monitoring, safety data review, protocol development, and providing clinical support to studies. The position also involves mentoring others and contributing to strategic discussions with key stakeholders.
This role involves overseeing the medical and scientific aspects of clinical trials in Internal Medicine, ensuring data integrity and quality. Responsibilities include medical monitoring, safety data review, protocol development, and providing clinical support to study teams and external stakeholders.
This role involves leading the development and execution of global evidence generation strategies to support patient access to Pfizer’s Obesity treatments. The Director will manage health economics and outcomes research, coordinate with cross-functional teams, and develop strategic partnerships to ensure successful reimbursement and market access.
The Director, HTA, Value & Evidence (HV&E) – Obesity will lead the development and execution of global evidence generation strategies to support patient access to Pfizer’s Obesity treatments. This involves managing health economics and outcomes research, coordinating with cross-functional teams, and developing strategic partnerships with external experts to ensure successful reimbursement and access requirements.
