94 jobs
Johnson & Johnson MedTech Maidenhead
Oversees local UK clinical trials from start-up through database lock, acting as the country-level point of contact and coordinating the local trial team to deliver compliant, high-quality data. Leads feasibility, site selection, recruitment planning and IRAS submissions, while mentoring CTAs and Site Managers and monitoring trial progress against timelines and budget.
Johnson & Johnson MedTech Raritan, United States US$137,000 – US$235,750 pa
Leads the Accelerando program management function, partnering with high-priority new product development teams to de-risk and accelerate clinical trial execution. Acts as a trusted advisor to Compound Development Teams, running critical path analysis, threat and opportunity assessments, and project planning in Planisware and MS Project. Also leads a team, drives best-practice adoption and benchmarking across a global matrix organisation.
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 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 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 Maidenhead
Leads preparation and finalisation of clinical documents within the Regulatory Medical Writing team, supporting the Immunology therapeutic area. Takes a lead role on assigned projects covering content, scientific strategy, timing and tracking, and manages direct reports including hiring, goal-setting and development. Involves mentoring junior writers, overseeing external contractors, and driving departmental process improvements.
Johnson & Johnson MedTech Beerse, Belgium €79,800 – €137,770 pa
Leads preparation and finalisation of clinical and regulatory documents for the Immunology therapeutic area within the Regulatory Medical Writing team. Acts as lead writer or point of contact for programmes, guides cross-functional teams, and manages, mentors and develops direct reports in medical writing.
Johnson & Johnson MedTech Leiden, Netherlands €68,600 – €119,600 pa
Leads preparation and finalisation of clinical and regulatory documents for the Immunology therapeutic area within the Regulatory Medical Writing team. Acts as lead writer or point of contact for programmes, guides cross-functional teams, and manages, mentors and develops direct reports including hiring and performance discussions.
Johnson & Johnson MedTech Toronto, Canada US$134,000 – US$184,000 pa
Leads preparation and finalisation of clinical documents within the Regulatory Medical Writing team, supporting the Immunology therapeutic area. Takes a lead role on assigned programmes, planning and directing writing groups, mentoring junior writers and overseeing external contractors. Also manages direct reports, setting objectives and running performance and development discussions.
Johnson & Johnson MedTech Spring House, United States US$117,000 – US$201,250 pa
Leads regulatory medical writing for the Immunology therapeutic area, preparing and finalizing clinical documents and serving as lead writer or point of contact for assigned programs. Manages direct reports, sets objectives, mentors junior writers and oversees external contractors, while driving process improvements and cross-functional coordination.
Johnson & Johnson MedTech Allschwil, Switzerland
Leads the preparation and finalisation of clinical documents within the Regulatory Medical Writing team, supporting the Immunology therapeutic area. Acts as lead writer or point of contact for assigned programmes, planning and directing writing groups while coaching junior staff and managing direct reports. Involves cross-functional collaboration, regulatory guideline knowledge and departmental process improvement.
Johnson & Johnson MedTech Raritan, United States US$117,000 – US$201,250 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 matrixed regulatory 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 Titusville, 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, timelines and scientific integrity, resolves labeling issues, and contributes to global labeling strategy and continuous process improvement within a matrix team.
Johnson & Johnson MedTech Toronto, Canada CA$87,000 – CA$140,300 pa
Writes and coordinates clinical and regulatory documents such as CSRs, IBs, protocols, summary documents, RMPs and briefing documents for oncology programmes. Leads cross-functional document planning and review meetings, sets timelines and strategies, and mentors junior writers while acting as lead writer on most compounds. Hybrid role with three days onsite weekly.
