Future Tech Jobs
Future Tech Jobs
The Training Manager role involves designing and delivering training programs for sales and clinical teams across Western Europe/EMEA, focusing on Medtronic's Patient Monitoring portfolio. You will collaborate with various stakeholders to ensure training initiatives align with business objectives and improve customer engagement and patient outcomes.
The Training Manager role involves designing and delivering impactful training programs for sales and clinical teams supporting the Patient Monitoring portfolio. You will partner with various stakeholders to ensure training initiatives align with strategic priorities and business objectives, contributing to improved customer engagement and better patient outcomes through industry-leading monitoring technologies.
This role involves leading the global Health Care Compliance program for Clinical Research, Medical Affairs, R&D, and Business Development. Responsibilities include strategic oversight, risk assessment, and ensuring compliance across various business activities, including mergers, acquisitions, and strategic partnerships.
This role involves leading the Order-to-Cash (OTC) process globally for DePuy Synthes, ensuring end-to-end process design, governance, and performance. The manager will partner with supply chain, finance, and commercial teams to drive continuous improvement, compliance, and operational excellence in a complex, regulated medical technology environment.
Life. Unlimited. At Smith+Nephew we design and manufacture technology that takes the limits off living.Looking for a year in industry where you can build real marketing experience, contribute to meaningful projects and learn from experts in a global medical technology...
This role involves critically reviewing promotional materials and performing systematic evaluations of clinical evidence to support the Sports Medicine business. The position also leads the development of evidence-based communication strategies, translating complex scientific data into accessible assets for various stakeholders.
This role involves overseeing clinical risk management for post-approval clinical trials, ensuring data integrity, patient safety, and compliance with regulatory requirements. Responsibilities include leading a team of CRM Representatives, conducting risk assessments, and developing mitigation strategies.
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.
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 R&D colleagues through regular review cycles.
The Senior Scientist Clinical Pharmacokinetics role involves leading the end-to-end execution of Phase 1 clinical pharmacology studies, including protocol development, data analysis, and report writing. Additional responsibilities include supporting all phases of drug development with noncompartmental analysis and contributing to regulatory submissions.
The Senior Scientist Clinical Pharmacokinetics role involves leading the end-to-end execution of Phase 1 clinical pharmacology studies, including protocol development, data analysis, and report writing. The role also supports non-compartmental analysis for all phases of drug development and ensures the quality and accuracy of pharmacokinetic/pharmacodynamic data.
The Senior Scientist Clinical Pharmacokinetics role involves developing and analyzing clinical pharmacology protocols, performing pharmacokinetic/pharmacodynamic data analysis, and contributing to clinical study reports and regulatory submissions. The role also includes supporting all phases of drug development, from Phase 1 to Phase 4, with a focus on non-compartmental analysis and ensuring the accuracy and timeliness of PK/PD data.
The VELYS Spine Clinical Specialist is responsible for leading the clinical introduction, adoption, and optimization of VELYS Spine robotics and navigation systems in spinal units across the UK. Key responsibilities include on-site clinical launches, in-theatre case support, structured education programs, and building strong relationships with surgical and hospital teams to ensure safe and effective use of the technology.
