Future Tech Jobs
Future Tech Jobs
This role involves shaping the competitive position of bladder and bowel neurostimulation therapies internationally. You will lead product launches, develop marketing strategies, and collaborate with cross-functional teams to drive growth and deliver measurable commercial results in a fast-evolving market.
This role involves shaping the competitive position of bladder and bowel neurostimulation therapies internationally. You will lead product launches, develop marketing strategies, and collaborate with sales, market development, and global marketing teams to drive growth and deliver measurable commercial results.
The Manager, Medical Writing, Immunology role involves preparing and finalizing clinical documents, leading team projects, and guiding cross-functional team members on processes and best practices. The position focuses on the Immunology therapeutic area and supports the development of transformational medicines for immunological disorders.
The Manager, Medical Writing, Immunology role involves preparing and finalizing clinical documents, leading cross-functional teams, and guiding team members on processes and best practices. The position focuses on the Immunology therapeutic area, with responsibilities including content and scientific strategy, project management, and process improvements.
Life. Unlimited. At Smith+Nephew we design and manufacture technology that takes the limits off living.We are looking for a Contract Excellence Lead for our International region to join our Commercial Centre of Excellence. In this influential role, you will shape...
Life. Unlimited. At Smith+Nephew we design and manufacture technology that takes the limits off living.We are looking for a Contract Excellence Lead for our International region to join our Commercial Centre of Excellence. In this influential role, you will shape...
The Spine and Biomaterials Marketing Manager will lead the marketing strategy for the Spine and Biomaterials portfolio across international regions, driving brand visibility and market penetration. Key responsibilities include strategic development, campaign activation, product launches, performance analysis, and cross-functional collaboration to optimize market impact.
The Experienced Clinical Programmer is responsible for overseeing or developing complex clinical data management activities, including data model specifications, data stream integrations, and transformation of source data to internal models. They create and execute edit check programs, listings, and reports to ensure data quality and compliance, and may lead in process and tool improvements.
The role involves designing and implementing advanced AI/ML methods for medical video and image understanding, focusing on endoscopy, ultrasound, and MRE. You will collaborate with clinicians and data scientists to develop robust, interpretable tools that enhance clinical decision-making and trial efficacy.
The EMEA HEMA Associate Manager supports the regional development and execution of Health Economics & Market Access activities across EMEA. Key responsibilities include coordinating EMEA initiatives, supporting evidence generation, and ensuring consistent market access strategies across multiple countries.
The Medical Science Liaison role involves providing scientific and medical support to key opinion leaders and internal teams, focusing on the Haematology franchise. You will work in the field, sharing knowledge and insights to optimize brand and therapy strategies, contributing to the development of innovative treatments.
The Specialist, Clinical Risk Management Oncology, works closely 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 risk management activities, maintain clinical quality plans, and communicate risk updates to stakeholders through regular review cycles.
The Specialist, Clinical Risk Management Oncology, 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 active participation in study activities, maintaining clinical quality plans, and facilitating regular risk reviews and updates.
The Specialist, Clinical Risk Management Oncology, 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 communicating risk updates to stakeholders 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, building benchmark datasets, and partnering with AI engineering teams to improve AI systems in specialized clinical contexts.
