Future Tech Jobs
Future Tech Jobs
As a Senior Technical Service Supervisor, you will manage a team of field service engineers, handle customer escalations, negotiate service contracts, and provide technical support. You will act as the main point of contact for local customers, commercial teams, and the field team, ensuring smooth communication and problem resolution.
The Affera Regional Clinical Educator role involves driving clinical excellence among Affera Mapping Specialists in the UK. Responsibilities include in-field training, coaching, and support for the rollout of the Affera Mapping System and other electrophysiology technologies. The role requires strong expertise in electrophysiology and cardiac mapping, as well as the ability to develop and deliver tailored training programs.
At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through...
At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through...
The Training Manager role involves designing and delivering impactful training programs for sales and clinical teams, focusing on the Patient Monitoring portfolio. You will collaborate with various stakeholders to ensure training initiatives align with strategic priorities and business objectives, directly contributing to improved customer engagement and patient outcomes through industry-leading monitoring technologies.
This role involves leading clinical programming activities for MedTech trials, focusing on data modeling, CDISC SDTM submissions, and developing reporting solutions for safety and compliance monitoring. The programmer will create and review specifications, implement data transformations, and ensure adherence to regulatory standards. Work includes both internal data review models and submission-ready deliverables.
This role involves leading clinical risk management across complex trials and programs, ensuring data integrity, patient safety, and regulatory compliance. The individual will drive risk-based oversight, support inspection readiness, and advise on quality issues and corrective actions in a global, cross-functional environment.
The Senior Analytical Monitor role involves conducting analytical monitoring activities for multiple clinical trials, ensuring compliance with regulations and company policies. Responsibilities include performing regular reviews, detecting issues early, and collaborating with Site Managers and Central Monitoring Managers to improve data reliability and site satisfaction.
The Lead Local Trial Manager is responsible for managing and overseeing clinical trials in the UK, ensuring compliance with protocols, SOPs, and regulatory standards. Key responsibilities include coordinating trial activities, maintaining high-quality data, and collaborating with internal and external stakeholders to deliver successful trials.
The Senior Local Trial Manager is responsible for overseeing clinical trials in the UK, ensuring compliance with protocols, SOPs, and regulatory standards. Key responsibilities include coordinating trial activities, managing site selection, and maintaining relationships with external and internal stakeholders. The role involves process improvement, mentoring team members, and delivering high-quality data.
The Senior Specialist, Clinical Risk Management, works closely with trial teams to identify, assess, and mitigate quality risks that could impact trial data integrity, patient safety, and regulatory compliance. Key responsibilities include coordinating data-driven risk oversight, maintaining clinical quality plans, and facilitating regular risk updates to R&D colleagues.
This role involves providing high-quality medical input and leadership in oncology, collaborating with cross-functional teams to drive medical strategy and patient outcomes. Responsibilities include building expertise in oncology, gathering field insights, and contributing to evidence generation and medical affairs projects.
The Lead Product Analyst will manage IT solutions for customer order experiences, collaborating with business and technology teams to deliver user-centric, industry-leading strategies. Key responsibilities include driving integration with commercial and supply chain systems, evaluating industry capabilities, and fostering a culture of innovation and talent development.
The Specialist, Clinical Risk Management Oncology, works with trial teams to identify, assess, and mitigate quality risks that could impact trial data integrity, patient safety, and regulatory compliance. They actively participate in study activities, maintain clinical quality plans, and communicate risk updates to R&D colleagues through regular review cycles.
This role involves developing evaluation frameworks and rubrics for AI agents in clinical operations and global development. Responsibilities include designing quality dimensions, running human evaluation protocols, and building benchmark datasets. The position requires a strong understanding of clinical operations, regulatory documentation, and AI systems.
