Latest MedTech Data Scientist Jobs

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, project leadership, and compliance with global regulatory standards. The manager will lead writing teams, mentor junior staff, and collaborate cross-functionally to ensure high-quality submissions. They will also contribute to process improvements and maintain alignment 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 within a global pharmaceutical environment, with a focus on cross-functional collaboration and scientific strategy. The manager will oversee writing teams, ensure compliance with regulatory standards such as ICH, and drive process improvements across therapeutic areas. Emphasis is placed on mentoring junior staff, managing complex timelines, and acting as a key liaison between clinical teams and regulatory stakeholders.

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 cross-functional environment, with a focus on scientific strategy, submission planning, and team leadership. The manager will guide medical writing activities across multiple therapeutic areas, mentor junior staff, and ensure compliance with regulatory standards such as ICH. The position operates in a hybrid model, requiring collaboration with global teams and active participation in process improvement initiatives.

Johnson & Johnson MedTech

Hybrid Permanent

Manager, Medical Writing, Immunology

This role involves leading the development and finalization of clinical and regulatory documents within the Immunology therapeutic area, with a focus on scientific strategy, team leadership, and cross-functional collaboration. The manager will oversee medical writing projects from planning to delivery, mentor junior staff, and ensure compliance with regulatory standards such as ICH guidelines. The position also includes direct people management, process improvement, and coordination across global teams in a patient-centered innovation environment.

Johnson & Johnson MedTech Switzerland

On-site Permanent

Manager, Medical Writing, Immunology

Lead and manage the creation of clinical and regulatory documents within the Immunology therapeutic area, providing scientific and strategic direction for medical writing teams. This role involves mentoring junior staff, driving process improvements, and ensuring compliance with regulatory standards. The position also includes direct people management responsibilities and cross-functional collaboration across drug development programs.

Johnson & Johnson MedTech Canada

Remote Permanent

Manager, Medical Writing, Immunology

Lead and manage medical writing activities for immunology clinical documents, including planning, authoring, and mentoring junior staff. Guide cross-functional teams, ensure regulatory compliance, and drive process improvements in a global healthcare environment.

Johnson & Johnson MedTech Belgium

On-site Permanent

Manager, Medical Writing, Immunology

Lead and manage the development of clinical and regulatory medical writing deliverables within the Immunology therapeutic area, providing scientific and strategic input across the product lifecycle. This role involves direct supervision of medical writers, mentoring junior staff, leading cross-functional writing teams, and ensuring compliance with regulatory standards. The position requires deep expertise in medical writing processes, ICH guidelines, and clinical documentation, with a strong emphasis on leadership, project management, and process improvement.

Johnson & Johnson MedTech

On-site Permanent

Medical Science Liaison

The Medical Science Liaison (MSL) will engage with Key Opinion Leaders and healthcare professionals in the haematology therapeutic area, providing scientific and medical expertise. This field-based role involves translating complex clinical data, supporting brand strategy through insights, and collaborating with cross-functional teams. The position offers the opportunity to contribute to Johnson & Johnson’s innovation in MedTech within a growing therapy area.

Johnson & Johnson MedTech High Wycombe, United Kingdom

Remote 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

Senior Site Manager (Senior Clinical Research Assistant)

This role involves managing oncology clinical trial sites from start-up to close-out, ensuring compliance with protocols, regulations, and data integrity. The Senior Site Manager acts as the main liaison between sponsor and site, conducting monitoring visits, supporting recruitment strategies, resolving issues, and maintaining inspection readiness across phases 2–4 trials. The position requires extensive travel and combines hands-on site management with collaboration across multidisciplinary teams.

Johnson & Johnson MedTech High Wycombe, United Kingdom

Hybrid Permanent

Lead MSA SOP Strategy & External Envir

This role leads the strategy and governance of Standard Operating Procedures (SOPs) for Medical and Scientific Affairs within DePuy Synthes, focusing on clinical research, Medical Affairs, and clinical evidence generation for orthopedic medical devices. The position ensures global regulatory compliance, drives SOP updates in response to evolving standards, and coordinates cross-functionally to maintain audit readiness and operational excellence across a highly regulated environment.

Johnson & Johnson MedTech Leeds, United Kingdom

Hybrid Permanent

Start Up Senior Trial Manager, Early Development

This role involves managing early development clinical trials in the UK, with dual responsibilities in trial oversight and study start-up activities. The candidate will coordinate local trial teams, ensure compliance with regulatory and ethical standards, manage UK regulatory submissions, and support efficient trial delivery from feasibility to close-out. The position bridges operational delivery and start-up functions, emphasizing process improvement, mentoring, and cross-functional collaboration in a hybrid work environment.

Johnson & Johnson MedTech High Wycombe, United Kingdom

Hybrid Permanent

Medical Writer III

This role involves writing and coordinating clinical and regulatory documents such as CSRs, protocols, and regulatory responses within the Immunology therapeutic area. The Medical Writer III leads document planning and review meetings with cross-functional teams, ensures compliance with internal processes, and mentors junior staff. The position operates in a hybrid work model with a focus on global collaboration and adherence to regulatory standards.

Johnson & Johnson MedTech United States US$109,000 – US$174,800 pa

Hybrid Permanent

Medical Writer III

This role involves writing and coordinating clinical and regulatory documents such as CSRs, protocols, and regulatory responses within the Immunology therapeutic area. The Medical Writer III will lead document planning and review meetings with cross-functional teams, ensure compliance with internal processes, and mentor junior staff. The position operates in a hybrid model with a focus on regulatory medical writing within a global, collaborative environment.

Johnson & Johnson MedTech £109,000 – £174,800 pa

Hybrid Permanent

Medical Writer III

This role involves writing and coordinating complex clinical and regulatory documents such as CSRs, protocols, and regulatory responses within the Immunology therapeutic area. The Medical Writer III leads document planning and review meetings with cross-functional teams, ensures scientific accuracy, and mentors junior staff. The position operates in a hybrid work model with a focus on process leadership and adherence to regulatory standards.

Johnson & Johnson MedTech US$109,000 – US$174,800 pa

Hybrid Permanent