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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

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

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

Manager, Clinical Research Med Affairs

The Manager, Clinical Research Med Affairs role involves providing strategic compliance leadership and practical guidance on clinical trials, investigator interactions, and scientific exchange. The role partners with global R&D, clinical research, and medical affairs teams to identify and mitigate compliance risks, ensuring ethical innovation and sound decision-making.

Johnson & Johnson MedTech Leeds, 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 writing projects under supervision.

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

Medical Advisor/Sr. Medical Advisor

This role involves providing high-quality medical input and leadership in oncology, collaborating with cross-functional teams to drive medical strategy and patient outcomes. Responsibilities include building expertise in oncology, gathering field insights, and contributing to evidence generation and medical affairs projects.

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

Medical Governance Manager

This role involves implementing and maintaining the UK medical governance framework, reviewing and certifying materials, and providing compliance training. The position is pivotal in ensuring high ethical standards and compliance with the ABPI Code of Practice, working closely with cross-functional teams.

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

Medical Writer II, Oncology

This role involves writing and coordinating clinical documents, such as Phase 1 protocols and clinical study reports, for oncology treatments. 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 United States
On-site Permanent

Medical Writer II, Oncology

This role involves writing and coordinating basic clinical documents such as Phase 1 protocols, Phase 1/2 CSRs, 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
Hybrid Permanent

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