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Manager, Medical Writing, Immunology

The Manager, Medical Writing, Immunology role involves preparing and finalizing clinical documents, leading team projects, and guiding cross-functional team members on processes and best practices. The position focuses on the Immunology therapeutic area and supports the development of transformational medicines for immunological disorders.

Johnson & Johnson MedTech Switzerland
On-site Permanent

Manager, Medical Writing, Immunology

The Manager, Medical Writing, Immunology role involves preparing and finalizing clinical documents, leading cross-functional teams, and guiding team members on processes and best practices. The position focuses on the Immunology therapeutic area, with responsibilities including content and scientific strategy, project management, and process improvements.

Johnson & Johnson MedTech Canada
Remote 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 Liverpool, 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. The role involves building strong stakeholder relationships, ensuring robust evidence for product approval and market access, and communicating scientific and clinical data effectively.

Johnson & Johnson MedTech Birmingham, 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. Key responsibilities include stakeholder engagement, evidence generation, and supporting regulatory and market access initiatives. The role involves deep engagement with the healthcare ecosystem to identify unmet needs and translate them into actionable insights.

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

Director, Clinical Risk Management Post Approval Delivery Unit

This role involves overseeing clinical risk management for post-approval clinical trials, ensuring data integrity, patient safety, and compliance with regulatory requirements. Responsibilities include leading a team of CRM Representatives, conducting risk assessments, and developing mitigation strategies.

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

Specialist Clinical Risk Management Oncology

The Specialist, Clinical Risk Management Oncology, 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 review cycles.

Johnson & Johnson MedTech United States
On-site Permanent

Specialist Clinical Risk Management Oncology

The Specialist, Clinical Risk Management Oncology, 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, maintaining clinical quality plans, and facilitating regular risk reviews and updates.

Johnson & Johnson MedTech
On-site Permanent

Specialist Clinical Risk Management Oncology

The Specialist, Clinical Risk Management Oncology, 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 communicating risk updates to stakeholders through regular review cycles.

Johnson & Johnson MedTech
On-site Permanent

Specialist, Clinical Risk Management Oncology

The Specialist, Clinical Risk Management Oncology, 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 communicating risk updates to R&D colleagues through regular review cycles.

Johnson & Johnson MedTech Belgium
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
On-site Permanent

Medical Writer II, Oncology

This role involves writing and coordinating clinical and regulatory documents for oncology treatments, including Phase 1-3 protocols, CSRs, and IB updates. The Medical Writer II will work in a team environment, applying internal standards and regulatory guidelines, and may lead writing projects under supervision.

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

Medical Writer II, Oncology

This role involves writing and coordinating clinical and regulatory documents for oncology treatments, including Phase 1-3 protocols, CSRs, and IB updates. The Medical Writer II will work in a team environment, applying internal standards and regulatory guidelines, and may lead on specific projects under supervision.

Johnson & Johnson MedTech Canada
Remote Permanent

Medical Writer II, Oncology

The Medical Writer II, Oncology role involves writing and coordinating clinical and regulatory documents, such as Phase 1-3 protocols, CSRs, and IB updates. You will work in a team environment, applying internal standards and regulatory guidelines, and participate in process working groups to support the development of oncology treatments.

Johnson & Johnson MedTech Switzerland
On-site Permanent

Medical Writer II, Oncology

This role involves writing and coordinating clinical and regulatory documents for oncology treatments, including Phase 1-3 protocols, clinical study reports, and initial IBs. The Medical Writer II will work in a team environment, applying internal standards and regulatory guidelines, and may lead writing projects under supervision.

Johnson & Johnson MedTech Belgium
On-site Permanent

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