Latest Clinical Research Associate Jobs

Lead, Trial Delivery Management

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through...

Johnson & Johnson MedTech High Wycombe, United Kingdom

Senior Analytical Monitor

The Senior Analytical Monitor role involves conducting analytical monitoring activities for multiple clinical trials, ensuring compliance with regulations and company policies. Responsibilities include performing regular reviews, detecting issues early, and collaborating with Site Managers and Central Monitoring Managers to improve data reliability and site satisfaction.

Johnson & Johnson MedTech High Wycombe, United Kingdom
Hybrid Permanent
Medtronic logo

Territory Manager Cardiac Ablation Solutions

This role involves developing and implementing sales and call plans for hospitals, providing technical expertise through sales presentations and product demonstrations, and offering training and support to medical professionals. The position focuses on maintaining and growing business in the Cardiac Ablation Solutions (CAS) market, particularly in Electrophysiology (EP).

Medtronic York, YO1 8RS, United Kingdom
On-site Permanent
Medtronic logo

Technical Consultant

As a Technical Consultant in the Cardiac Ablation Solutions (CAS) team, you will provide technical support, training, and education to customers, ensuring the successful introduction and market release of new products. Your role involves working closely with the clinical team, sales, and marketing to enhance Medtronic’s reputation and meet business targets.

Medtronic Cambridge, United Kingdom £42,000 – £63,000 pa
On-site Permanent

Lead, Trial Delivery Management

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through...

Johnson & Johnson MedTech Canada

Lead, Trial Delivery Management

This role involves leading the execution of clinical trial activities, including managing trial-specific documentation, overseeing vendor operations, and coordinating country or regional trial management efforts. The position requires input into operational strategies, risk mitigation, and support for compound training development, with a focus on ensuring compliance and efficient study delivery across global teams. It also includes mentoring team members and contributing to process improvements across clinical trial functions.

Johnson & Johnson MedTech United States
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

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 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

Medical Writer II, Oncology

The Medical Writer II, Oncology role involves writing and coordinating clinical documents such as Phase 1 protocols, Phase 1/2 CSRs, and initial IBs. You will work in a team environment, applying internal standards and regulatory guidelines, and may lead writing projects under supervision.

Johnson & Johnson MedTech
Hybrid 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