201 jobs
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 Copenhagen, Denmark
Supports the Medical Affairs team on intraocular lens (IOL) proctoring and Medical Information requests, analysing surgical cases and sub-optimal outcomes to optimise clinical results. Handles MIR responses within four days, produces statistics reports, and assists HCPs with post-operative analysis and new product introductions. Home-office based with up to 20% travel across EMEA.
Johnson & Johnson MedTech Stockholm, Sweden
Supports the Medical Affairs team for intraocular lenses, analysing surgical cases and calculations, managing medical information requests within four days, and helping clinicians optimise post-operative outcomes. Works closely with Product Safety, Marketing, R&D and Commercial on clinical performance reporting and new product introductions, with home-office working and up to 20% travel.
Johnson & Johnson MedTech Pomezia, Roma, Italy
Supports intraocular lens proctoring and medical information requests, analysing surgical cases and sub-optimal outcomes to optimise clinical use of ophthalmic products. Handles MIR responses within four days, produces statistics reports, and assists HCPs with post-operative analysis and new product introductions. Home-office based with up to 20% travel across EMEA.
Johnson & Johnson MedTech London
Supports the Medical Affairs team with intraocular lens proctoring and medical information requests, analysing surgical cases and sub-optimal outcomes to optimise product use. Provides clinical expert support to healthcare professionals on post-operative outcomes, new product introductions, demos and clinical studies, working closely with Product Safety, Marketing, R&D and Commercial. Home-office based with up to 20% travel across EMEA.
Johnson & Johnson MedTech Limerick, Ireland
Supports intraocular lens proctoring and medical information requests, analysing surgical cases and post-operative outcomes to optimise clinical results. Collaborates with product safety, marketing, R&D and commercial teams, providing expert support to healthcare professionals and internal customers on new product introductions. Home-office based with up to 20% travel across EMEA.
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.
Johnson & Johnson MedTech Raritan, United States US$137,000 – US$235,750 pa
Leads scientific safety assessments for assigned medicinal products, partnering with Medical Safety Officers to prepare regulatory safety analyses and benefit-risk evaluations. Supports Safety Management Teams, chairs proactive safety data reviews, and acts as product SME for audits and health authority interactions.
Johnson & Johnson MedTech Horsham, United States US$137,000 – US$235,750 pa
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, chairs proactive safety data reviews, and acts as product or process subject matter expert for audits and health authority interactions.
Johnson & Johnson MedTech Titusville, United States US$137,000 – US$235,750 pa
Leads scientific safety assessments for assigned medicinal products, partnering with Medical Safety Officers to prepare regulatory safety analyses and evaluations. Supports Safety Management Teams, conducts proactive safety data reviews, and serves as product point of contact, with oversight of deliverables prepared by other team members.
Johnson & Johnson MedTech Maidenhead
Lead a two-year postdoctoral research program on making agentic AI safe for pharmaceutical R&D, covering provable controls, adversarial assurance, and safety-native architecture. You will design reproducible experiments, prototype layered safeguards, publish results, and work with platform engineers to move validated methods into a GenAI platform.
Johnson & Johnson MedTech Limerick, Ireland
Lead a two-year postdoctoral research program on making agentic AI safe for pharmaceutical R&D, covering provable controls, adversarial assurance and safety-native architecture. Hands-on work prototyping and validating methods on real GenAI platform workflows, publishing results and handing validated approaches to engineering partners.
Johnson & Johnson MedTech Beerse, Belgium
Lead a two-year postdoctoral research program on making agentic AI safe for regulated pharmaceutical R&D, covering provable controls, adversarial assurance, and safety-native architecture. You will design reproducible experiments, prototype layered architectures, and work with platform engineers to move validated methods into a GenAI platform. The role is hands-on research with real systems as the testbed, not frontier model pre-training or production engineering.
Johnson & Johnson MedTech Leiden, Netherlands
Lead a two-year postdoctoral research program on making agentic AI safe for pharmaceutical R&D, covering provable controls, continuous adversarial red-teaming, and safety-native architecture. Hands-on work prototyping and validating methods on real GenAI platform workflows, publishing results, and transitioning validated approaches into production with engineering partners.
