Latest Project Services Jobs

Manager, Global Transparency Reporting - EMEA

Lead end-to-end global transparency reporting operations across EMEA, ensuring compliance with evolving regulations and industry codes. Manage a team, drive process improvements, and collaborate with cross-functional stakeholders to enhance data quality and reporting efficiency. Leverage digital tools and automation to scale compliance capabilities and deliver actionable insights through analytics and visualization.

Johnson & Johnson MedTech €79,800 – €137,770 pa

Manager, Global Transparency Reporting - EMEA

Lead end-to-end global transparency reporting operations across EMEA, ensuring compliance with evolving regulations and industry codes. Manage a team, drive process improvements, and collaborate with cross-functional stakeholders to enhance data quality and reporting accuracy. Leverage digital tools and analytics to identify risks and deliver compliance insights.

Johnson & Johnson MedTech

Senior Clinical Research Specialist

Manages Investigator-Sponsored Research (ISR) studies from initiation to close-out, ensuring compliance with GCP and regulatory standards. Oversees device logistics, financial administration, and contract coordination across global surgical business units. Acts as a European representative on the global ISR Council and leads process improvements in clinical research operations.

Medtronic London, United Kingdom £50,400 – £75,600 pa

Senior Clinical Research Specialist

Manages Investigator-Sponsored Research (ISR) studies from initiation to close-out, ensuring compliance with GCP and regulatory standards. Supports clinical documentation, financial administration, and device logistics across global Surgical business units. Acts as a European representative on the global ISR Council and leads process improvements in contracting, payments, and compliance workflows.

Medtronic £50,400 – £75,600 pa

Manager, Global Transparency Reporting - EMEA

Lead and manage end-to-end global transparency reporting for the EMEA region, ensuring compliance with evolving regulations and industry standards. Oversee data collection, validation, and submission processes while driving process improvements and leading a team. Collaborate with cross-functional stakeholders to enhance reporting accuracy, implement automation, and deliver data-driven insights to support compliance and risk management.

Johnson & Johnson MedTech Greece

On-site Permanent

Medical Writer II, X-TA

This role involves authoring and coordinating regulatory medical writing documents across key therapeutic areas such as Oncology, Immunology, and Neuroscience. The Medical Writer II will produce clinical study reports, protocols, and investigational brochures, ensuring compliance with ICH guidelines and internal standards. They will collaborate with cross-functional teams, contribute to document planning and review, and support quality control processes while adhering to regulatory and scientific best practices.

Johnson & Johnson MedTech High Wycombe, United Kingdom

Hybrid Permanent

Manager Regulatory Medical Writing X-TA

This role involves leading the preparation and finalization of clinical regulatory documents across multiple therapeutic areas, with a focus on strategic input, cross-functional collaboration, and compliance with global regulatory standards. The individual will lead writing teams, mentor junior staff, and drive process improvements within the medical writing function. Based in a hybrid work model, the position requires strong scientific communication skills and deep familiarity with ICH and other regulatory guidelines.

Johnson & Johnson MedTech Netherlands €68,600 – €119,600 pa

Hybrid Permanent

Manager Regulatory Medical Writing X-TA

This role involves leading the preparation and finalization of clinical and regulatory documents across multiple therapeutic areas, with a focus on strategic input, scientific accuracy, and compliance with regulatory standards. The manager will lead writing teams, mentor junior staff, and collaborate cross-functionally to ensure high-quality submissions. The position operates in a hybrid model, requiring onsite presence while supporting global regulatory initiatives.

Johnson & Johnson MedTech €60,400 – €103,960 pa

Hybrid Permanent

Manager Regulatory Medical Writing X-TA

Leads the preparation and finalization of clinical and regulatory documents across multiple therapeutic areas, providing scientific and strategic direction for writing teams. Manages timelines, mentors junior staff, and ensures compliance with regulatory standards such as ICH guidelines. Operates with high independence while collaborating closely with cross-functional teams to deliver high-quality medical content for submissions.

Johnson & Johnson MedTech €79,800 – €137,770 pa

Hybrid Permanent

Manager Regulatory Medical Writing X-TA

This role involves leading the preparation and finalization of clinical and regulatory documents within a global medical writing team, with a focus on cross-functional collaboration and scientific strategy. The individual will guide teams, ensure compliance with regulatory standards such as ICH, and mentor junior staff. Based in a hybrid work model, the position supports multiple therapeutic areas and drives process improvements in medical writing operations.

Johnson & Johnson MedTech €78,300 – €135,700 pa

Hybrid Permanent

Medical Writer II, X-TA

A Medical Writer II in Regulatory Medical Writing will author and coordinate clinical and regulatory documents across therapeutic areas such as Oncology, Immunology, and Neuroscience. The role involves drafting protocols, clinical study reports, and regulatory submissions while collaborating with cross-functional teams. The position operates in a hybrid model with 3 days onsite weekly and requires strong scientific writing skills and familiarity with regulatory guidelines.

Johnson & Johnson MedTech Belgium €60,000 – €97,865 pa

Hybrid Permanent

Medical Writer II, X-TA

This role involves authoring and coordinating regulatory medical writing documents such as clinical study reports, protocols, and investigator brochures across key therapeutic areas including Oncology, Immunology, and Neuroscience. The Medical Writer II will work within a cross-functional team to ensure accurate, high-quality documentation in compliance with regulatory standards and internal guidelines, while also mentoring junior staff and contributing to process improvements. The position operates in a hybrid model with a mix of on-site and remote work.

Johnson & Johnson MedTech

Hybrid Permanent

Medical Advisor

The Medical Advisor in Oncology provides scientific leadership and strategic input to support patient outcomes and healthcare professionals within the NHS. This role involves deep engagement with clinicians and academics, contributing to evidence generation, medical strategy, and cross-functional collaboration across Medical Affairs, Market Access, and Commercial teams. The advisor also supports advisory boards, medical education, and HTA submissions while ensuring compliance with ABPI standards.

Johnson & Johnson MedTech High Wycombe, United Kingdom

Associate Development Engineer

Design and develop new hip implants and surgical instruments within a multidisciplinary R&D team, focusing on feasibility, manufacturability, and transfer to production. Perform engineering analyses including FEA and tolerance studies, support verification/validation planning, and collaborate with manufacturing and supply chain partners. Work in a regulated medical device environment with exposure to design excellence methodologies and global teams.

Johnson & Johnson MedTech Leeds, United Kingdom

Manager Regulatory Medical Writing XTA

Leads the preparation and finalization of clinical regulatory documents, providing scientific and strategic direction for medical writing teams. Provides mentorship, drives process improvements, and serves as a key liaison between cross-functional teams and regulatory stakeholders. Works independently on complex projects across multiple therapeutic areas.

Johnson & Johnson MedTech High Wycombe, United Kingdom

Hybrid Permanent