Jobs in Exeter

Principal C&SP Methodology Lead

The Principal C&SP Methodology Lead is a senior technical role responsible for driving innovation and implementing solutions in clinical and statistical programming. The role involves leading projects, developing tools, and coaching team members to enhance automation, efficiency, and quality in data management and analysis.

Johnson & Johnson MedTech

Principal C&SP Methodology Lead

The Principal C&SP Methodology Lead is a senior technical role responsible for driving innovation and technical strategy in clinical and statistical programming. The role involves developing and implementing cutting-edge solutions to improve data management, automation, and regulatory compliance, while also providing leadership and training to departmental staff.

Johnson & Johnson MedTech

Associate Director, Clinical Risk Management

This role involves leading clinical risk management across multiple therapeutic areas, focusing on identifying, assessing, and mitigating quality risks in clinical trials to ensure patient safety, data integrity, and regulatory compliance. The individual will drive risk-based oversight, support inspection readiness, lead quality investigations, and advise on CAPA plans in a global, cross-functional environment. Key activities include coaching teams, maintaining clinical quality plans, and contributing to governance forums to uphold high standards in clinical development.

Johnson & Johnson MedTech

Hybrid Permanent

Associate Dir. Cross TA Risk Management

This role leads clinical risk management across therapeutic areas in J&J's R&D organization, focusing on ensuring data integrity, patient safety, and regulatory compliance in clinical trials. The individual will drive risk-based oversight, support inspection readiness, and provide expert guidance on quality issues and CAPA plans. The position operates in a global, cross-functional environment and contributes to shaping quality systems and processes across clinical development.

Johnson & Johnson MedTech United States US$122,000 – US$212,750 pa

Hybrid Permanent

Associate Dir. Cross TA Risk Management

This role involves leading clinical risk management across therapeutic areas, ensuring data integrity, patient safety, and regulatory compliance in global clinical trials. The Associate Director drives risk-based oversight, inspection readiness, and quality governance, working closely with cross-functional teams to identify, assess, and mitigate risks throughout trial lifecycles. They also support audits, inspections, and the development of corrective actions, contributing to a robust quality framework in R&D.

Johnson & Johnson MedTech US$122,000 – US$212,750 pa

Hybrid Permanent

Associate Dir. Cross TA Risk Management

This role involves leading clinical risk management across therapeutic areas, ensuring data integrity, patient safety, and regulatory compliance in global clinical trials. The Associate Director will drive risk-based oversight, inspection readiness, and quality investigations, while advising trial teams and collaborating with cross-functional stakeholders to maintain high standards in clinical research quality.

Johnson & Johnson MedTech US$122,000 – US$212,750 pa

Hybrid Permanent

Associate Dir. Cross TA Risk Management

This role involves leading clinical risk management across therapeutic areas, ensuring trial data integrity, patient safety, and regulatory compliance. The individual will drive risk-based oversight, develop Clinical Quality Plans, support inspection readiness, and advise on quality issues and CAPAs in a global, cross-functional environment.

Johnson & Johnson MedTech US$122,000 – US$212,750 pa

Hybrid Permanent

Assoc Director, Clinical Risk Management

This role involves leading clinical risk management activities across therapeutic areas, focusing on identifying, assessing, and mitigating quality risks in clinical trials to ensure patient safety, data integrity, and regulatory compliance. The individual will drive risk-based monitoring, support inspection readiness, lead quality investigations, and provide expert guidance on GCP, CAPA, and regulatory standards within a global, cross-functional R&D environment.

Johnson & Johnson MedTech Switzerland

Hybrid Permanent

Director, Regulatory Data Office Leader

This role involves leading a global team of data stewards and overseeing the Regulatory Data Hub to ensure high-quality regulatory data for business intelligence and decision-making. The Director will establish data governance policies, collaborate across R&D and IT, and drive regulatory data transformation initiatives.

Johnson & Johnson MedTech High Wycombe, United Kingdom

Senior Manager/Associate Director Clinical Data Transparency, EHDS Data Cataloguing

This role involves leading the EHDS Data Inventory and Cataloguing workstream, coordinating data owners across functions, and maintaining a standardized and discoverable view of J&J's in-scope health data. Responsibilities include applying metadata standards, developing classification guidance, and embedding sustainable processes for data governance.

Johnson & Johnson MedTech High Wycombe, United Kingdom

Director, Regulatory Data Office Leader

The Director, Regulatory Data Office Leader, will lead a global team of data stewards and oversee the Regulatory Data Hub (RDH) to ensure high-quality regulatory data for business intelligence and decision-making. The role involves data governance, regulatory compliance, and collaboration with R&D, IT, and data science teams to drive digital transformation and AI adoption.

Johnson & Johnson MedTech

Snr Mgr / AD EHDS Data Cataloguing

This role involves leading the identification, classification, and cataloging of health data under the European Health Data Space (EHDS) for Johnson & Johnson. The Senior Manager / Associate Director will coordinate with data owners, apply metadata standards, and ensure the completeness and consistency of the data catalog, working closely with legal, privacy, and technology teams.

Johnson & Johnson MedTech Switzerland

Director, Regulatory Data Office Leader

The Director, Regulatory Data Office Leader, will lead a global team of data stewards and oversee the Regulatory Data Hub (RDH) to ensure high-quality regulatory data for business intelligence and decision-making. Key responsibilities include data governance, regulatory data council leadership, and transformation enablement through digital solutions and AI.

Johnson & Johnson MedTech United States £150,000 – £258,750 pa

Services and Solutions Manager | J&J MedTech

The Services and Solutions Manager will lead the deployment of value offerings to drive market share with strategic customers, focusing on clinical transformation, theatre efficiency, and patient pathway programmes. The role involves managing relationships with NHS trusts and private sector organisations, mentoring consultants, and reporting on key performance indicators.

Johnson & Johnson MedTech United Kingdom

Medical Writer II, X-TA

The Medical Writer II, Regulatory Medical Writing role involves authoring and coordinating clinical and regulatory documents for various therapeutic areas. Responsibilities include writing Phase 1-3 protocols, clinical study reports, and regulatory responses, as well as participating in cross-functional document planning and review meetings. The role requires strong scientific and regulatory writing skills, attention to detail, and the ability to work in a team environment.

Johnson & Johnson MedTech