96 jobs
Johnson & Johnson MedTech Breda, Netherlands €64,000 – €103,040 pa
Supports Clinical Trial Management Solutions (CTMS, Site Payments, Access Provisioning) as a liaison between business teams, IT and suppliers. Handles study build, system integrations, release management, UAT, end-user support and training, plus automation, analytics and GenAI improvements. Hybrid role with up to 10% travel.
Johnson & Johnson MedTech Leiden, Netherlands €64,000 – €103,040 pa
Supports Clinical Trial Management Solutions (CTMS, Site Payments, Access Provisioning) as a liaison between business teams, IT and suppliers. Handles study build, release management, UAT, integrations, end-user support and audits, and drives automation, analytics and GenAI improvements. Hybrid working with up to 10% international travel.
Smith & Nephew Luton
Owns and grows a strategic orthopaedic revision territory from the M1 corridor to the East of England, supporting complex surgical cases in theatre and building relationships with surgeons and theatre teams. Drives new business, account plans, tenders and adoption of advanced technologies including robotics, working alongside Account Managers and Area Business Managers.
Smith & Nephew Peterborough
Field-based role owning a strategic orthopaedic revision territory from the M1 corridor to the East of England, supporting complex surgical cases in theatre and building relationships with surgeons and theatre teams. Combines clinical expertise with commercial account planning, tenders and product introductions, including advanced technologies such as robotics.
Johnson & Johnson MedTech Spring House, United States US$109,000 – US$174,800 pa
Supports Clinical Trial Management Solutions (CTMS, Site Payments, Access Provisioning) as a liaison between business, IT and suppliers. Executes system improvements, study build and maintenance, end-user support, release management, UAT and integrations, and explores automation, analytics and GenAI opportunities. Also delivers training and supports audits and regulatory inspections.
Johnson & Johnson MedTech Raritan, United States US$109,000 – US$174,800 pa
Supports Clinical Trial Management Solutions (CTMS, Site Payments, Access Provisioning) as a liaison between business, IT and suppliers. Handles study build, system integrations, release management, UAT, end-user support and audits, while driving automation, analytics and GenAI improvements. Requires 5+ years in clinical trial execution and GCP knowledge.
Johnson & Johnson MedTech Beerse, Belgium €72,500 – €115,230 pa
Supports Clinical Trial Management Solutions (CTMS, Site Payments, Access Provisioning) as a liaison between business teams, IT and suppliers. Handles study build, system integrations, release management, UAT, end-user support and training, plus automation, analytics and GenAI improvements. Requires 5+ years in clinical trial execution and GCP knowledge.
Johnson & Johnson MedTech Horsham, United States US$109,000 – US$174,800 pa
Supports Clinical Trial Management Solutions (CTMS, Site Payments, Access Provisioning) as a liaison between business, IT and suppliers. Handles study build, release management, user acceptance testing, integrations, end-user support and audits, while driving automation, analytics and GenAI improvements. Requires 5+ years in clinical trial execution and GCP knowledge.
Johnson & Johnson MedTech High Wycombe
Leads the development, revision and maintenance of primary labeling documents such as the Company Core Data Sheet, US Package Insert and EU Product Information for assigned compounds. Advises on labeling content, processes and timelines, resolves labeling issues and contributes to global labeling strategy and continuous process improvement within a matrix team.
Johnson & Johnson MedTech Maidenhead
Leads scientific safety assessments for assigned medicinal products, partnering with Medical Safety Officers to prepare analyses and evaluations for regulatory compliance. Supports Safety Management Teams, conducts proactive safety data reviews, and acts as product point of contact, with hybrid working requiring three days on site.
Johnson & Johnson MedTech Breda, Netherlands €68,600 – €119,600 pa
Oversees the end-to-end process for internal and external clinical data sharing requests, ensuring compliance with privacy standards and procedures. Manages vendors handling anonymisation and synthetisation, and acts as the primary contact for YODA Project requests, supporting external research teams using clinical study data.
Johnson & Johnson MedTech Maidenhead
Supports Clinical Trial Management Solutions including CTMS, Site Payments and Access Provisioning, acting as liaison between business partners, IT and suppliers. Handles study build, system integrations, release management, user acceptance testing, end-user support and audits, while identifying automation, analytics and GenAI improvements. Requires deep clinical development and GCP knowledge.
Johnson & Johnson MedTech Zug, Switzerland
Leads the development, revision and maintenance of primary labeling documents including the Company Core Data Sheet, US Package Insert and EU Product Information for assigned compounds. Advises on labeling content, processes and timelines, resolves labeling issues, and contributes to global labeling strategy and continuous process improvement within a matrix team.
Johnson & Johnson MedTech Horsham, United States US$117,000 – US$201,250 pa
Leads the development, revision and maintenance of primary labeling documents including the Company Core Data Sheet, US Package Insert and EU Product Information for assigned compounds. Advises on labeling content, processes and timelines, resolves labeling issues, and contributes to global labeling strategy and continuous process improvement within a matrixed regulatory affairs team.
Johnson & Johnson MedTech Warsaw, Poland €205,000 – €354,200 pa
Leads the development, revision and maintenance of primary labeling documents such as the Company Core Data Sheet, US Package Insert and EU Product Information for assigned compounds. Advises on labeling content, processes and timelines, resolves labeling issues and contributes to global labeling strategy and continuous process improvement within a matrix team.
