Future Tech Jobs
Future Tech Jobs
In this role, you will shape the competitive strategy for bladder and bowel neurostimulation therapies, driving international product launches and marketing plans. You will collaborate with sales, market development, and global marketing teams to ensure successful execution and measurable business impact.
This role involves shaping the competitive position of bladder and bowel neurostimulation therapies internationally. Responsibilities include leading product launches, developing marketing strategies, and collaborating with sales, market development, and global marketing teams to drive growth and ensure successful go-to-market execution.
This role involves preparing and finalizing clinical documents for the Immunology therapeutic area, leading cross-functional teams, and guiding team members on processes and best practices. The Manager will work with a high level of independence, take a lead role in content and scientific strategy, and proactively recommend process improvements.
This role involves preparing and finalizing clinical documents, leading cross-functional teams, and guiding team members on processes and best practices. The Manager will work independently, take a lead role in content and scientific strategy, and drive departmental process improvements.
Life. Unlimited. At Smith+Nephew we design and manufacture technology that takes the limits off living.Join us as a Cluster Business Analyst and play a key role in shaping how our commercial teams make decisions. This is a great opportunity to...
Life. Unlimited. At Smith+Nephew we design and manufacture technology that takes the limits off living.We are currently searching for aSenior Productivity & Cost Optimisation Engineer.The Senior Productivity & Cost Optimisation Engineer is a strategic, technically grounded professional responsible for identifying,...
This role involves achieving sales targets for orthopaedic and neurological products in South Wales and Bristol. You will interact with key stakeholders in secondary care, develop business plans, and promote new technologies while maintaining strong customer relationships.
This role involves achieving sales targets for orthopaedic and neurological products in South Wales and Bristol. Responsibilities include building relationships with key stakeholders, promoting new technologies, and developing business plans to grow the company's market share.
This role involves providing in-theatre support to orthopaedic consultants and nursing staff, ensuring the correct use of DePuy Synthes products, and developing business opportunities across key accounts. The Clinical Specialist will also assist in training, customer education, and supporting medical education events, while maintaining strong relationships with clinical partners and key opinion leaders.
The Sales Specialist role involves achieving sales targets and promoting orthopedic and trauma products to key stakeholders in secondary care. Responsibilities include managing territory business plans, developing customer relationships, and driving the adoption of new technologies while maintaining core business.
The VELYS Trauma Marketing Manager will lead the launch and establishment of the new VELYS Trauma system within the DPS International business and Trauma Platforms. Key responsibilities include developing and executing international strategies, partnering with cross-functional teams, and ensuring market access and clinical evidence strategies are in place.
The Experienced Statistical Programmer is responsible for developing, verifying, and documenting code for clinical data analysis and reporting. They work on tasks of medium to high complexity, ensuring quality and timeliness, and collaborate with cross-functional teams to achieve project goals.
The Director, Major Markets Europe & Canada, provides strategic regulatory leadership across key European and Canadian markets. This role ensures compliance with local and regional regulatory requirements, manages regulatory risk, and supports business growth in highly regulated markets. Key responsibilities include leading regulatory affairs strategy, ensuring compliance, and partnering with cross-functional teams to manage product registrations and lifecycle management.
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 Associate Director, Regulatory Policy, provides leadership in regulatory compliance and policy, ensuring alignment with global and regional requirements. Key responsibilities include interpreting regulatory policies, developing internal guidelines, and supporting cross-functional teams to manage regulatory risks and enable informed decision-making.
