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Latest MedTech Data Scientist Jobs

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Manager, Medical Writing, Immunology

This role involves preparing and finalizing clinical documents for the Immunology therapeutic area, leading cross-functional teams, and guiding team members on processes and best practices. The Manager will work with a high level of independence, take a lead role in content and scientific strategy, and proactively recommend process improvements.

Johnson & Johnson MedTech Belgium
On-site Permanent

Manager, Medical Writing, Immunology

This role involves preparing and finalizing clinical documents, leading cross-functional teams, and guiding team members on processes and best practices. The Manager will work independently, take a lead role in content and scientific strategy, and drive departmental process improvements.

Johnson & Johnson MedTech
On-site Permanent

Medical Science Liaison

The Medical Science Liaison role involves providing scientific and medical support to key opinion leaders and internal teams, focusing on the Haematology franchise. You will work in the field, sharing knowledge and insights to optimize brand and therapy strategies, contributing to the development of innovative treatments.

Johnson & Johnson MedTech High Wycombe, United Kingdom
Remote Permanent

Manager, Medical Writing, Immunology

This role involves preparing and finalizing clinical documents for the Immunology therapeutic area, leading cross-functional teams, and guiding team members on processes and best practices. The Manager will work with a high level of independence, take a lead role on assigned projects, and recommend departmental process improvements.

Johnson & Johnson MedTech United States
On-site Permanent

Lead Local Trial Manager

The Lead Local Trial Manager is responsible for managing and overseeing clinical trials in the UK, ensuring compliance with protocols, SOPs, and regulatory standards. Key responsibilities include coordinating trial activities, maintaining high-quality data, and collaborating with internal and external stakeholders to deliver successful trials.

Johnson & Johnson MedTech High Wycombe, United Kingdom
Hybrid Permanent

Senior Local Trial Manager

The Senior Local Trial Manager is responsible for overseeing clinical trials in the UK, ensuring compliance with protocols, SOPs, and regulatory standards. Key responsibilities include coordinating trial activities, managing site selection, and maintaining relationships with external and internal stakeholders. The role involves process improvement, mentoring team members, and delivering high-quality data.

Johnson & Johnson MedTech High Wycombe, United Kingdom
Hybrid Permanent

Senior Specialist, Clinical Risk Management

The Senior Specialist, Clinical Risk Management, works closely with trial teams to identify, assess, and mitigate quality risks that could impact trial data integrity, patient safety, and regulatory compliance. Key responsibilities include coordinating data-driven risk oversight, maintaining clinical quality plans, and facilitating regular risk updates to R&D colleagues.

Johnson & Johnson MedTech High Wycombe, United Kingdom
On-site Permanent

Senior Specialist, Clinical Risk Management

The Senior Specialist, Clinical Risk Management, works closely with trial teams to identify, assess, and mitigate quality risks that could impact trial data integrity, patient safety, and regulatory compliance. Responsibilities include active participation in study activities, regular risk reviews, maintaining clinical quality plans, and communicating risk updates to stakeholders.

Johnson & Johnson MedTech United States
On-site Permanent

Senior Specialist, Clinical Risk Management

The Senior Specialist, Clinical Risk Management, works closely with trial teams to identify, assess, and mitigate quality risks that could impact trial data integrity, patient safety, and regulatory compliance. They actively participate in risk management activities, maintain clinical quality plans, and communicate risk updates to stakeholders through regular reviews and governance meetings.

Johnson & Johnson MedTech
On-site Permanent

Senior Specialist, Clinical Risk Management

The Senior Specialist, Clinical Risk Management, works closely with trial teams to identify, assess, and mitigate quality risks that could impact trial data integrity, patient safety, and regulatory compliance. Key responsibilities include active participation in study activities, regular risk reviews, maintaining clinical quality plans, and facilitating risk updates to R&D colleagues.

Johnson & Johnson MedTech
On-site Permanent

Senior Specialist, Clinical Risk Management

The Senior Specialist, Clinical Risk Management, works closely with trial teams to identify, assess, and mitigate quality risks that could impact trial data integrity, patient safety, and regulatory compliance. Responsibilities include active participation in study activities, maintaining clinical quality plans, and facilitating regular risk reviews and updates.

Johnson & Johnson MedTech
On-site Permanent

Senior Specialist, Clinical Risk Management

The Senior Specialist, Clinical Risk Management, collaborates with trial teams to identify, assess, and mitigate quality risks that could impact trial data integrity, patient safety, and regulatory compliance. Key responsibilities include participating in risk assessments, maintaining clinical quality plans, and communicating risk updates to R&D colleagues through regular review cycles.

Johnson & Johnson MedTech Belgium
On-site Permanent

Specialist, Clinical Risk Management Oncology

The Specialist, Clinical Risk Management Oncology, works with trial teams to identify, assess, and mitigate quality risks that could impact trial data integrity, patient safety, and regulatory compliance. They actively participate in study activities, maintain clinical quality plans, and communicate risk updates to R&D colleagues through regular review cycles.

Johnson & Johnson MedTech High Wycombe, United Kingdom
On-site Permanent

Medical Affairs Director | Johnson and Johnson| MedTech|UK

The Medical Affairs Director UK is a strategic leader responsible for shaping commercial strategy and driving innovation by leveraging deep surgical expertise and insights into the local healthcare ecosystem. Key responsibilities include stakeholder engagement, evidence strategy, and scientific leadership to support regulatory approval, market access, and clinical adoption of J&J MedTech products.

Johnson & Johnson MedTech Leeds, United Kingdom
On-site Permanent

Medical Affairs Director | Johnson and Johnson| MedTech|UK

The Medical Affairs Director UK is a strategic leader responsible for shaping commercial strategy and driving innovation by leveraging deep surgical expertise and insights into the local healthcare ecosystem. Key responsibilities include stakeholder engagement, evidence strategy, and scientific leadership to support regulatory approval, market access, and clinical adoption of J&J MedTech products.

Johnson & Johnson MedTech London, United Kingdom
On-site Permanent

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