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.
This role involves shaping the competitive landscape for bladder and bowel neurostimulation therapies, leading international product launches, and developing marketing strategies for the Pelvic Health business. You will collaborate with cross-functional teams to ensure successful market entry and drive growth through strategic initiatives and customer engagement.
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.
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.
This role involves writing and coordinating clinical documents, such as Phase 1 protocols and clinical study reports, for oncology treatments. The Medical Writer II will work in a team environment, applying internal standards and regulatory guidelines, and may lead writing projects under supervision.
This role involves writing and coordinating basic clinical documents such as Phase 1 protocols, Phase 1/2 CSRs, and initial IBs. The Medical Writer II will work in a team environment, applying internal standards and regulatory guidelines, and may lead writing projects under supervision.
The Medical Writer II, Oncology role involves writing and coordinating clinical documents such as Phase 1 protocols, Phase 1/2 CSRs, and initial IBs. You will work in a team environment, applying internal standards and regulatory guidelines, and may lead writing projects under supervision.
The Manager, Safety Analysis Scientist role involves leading the safety assessment of assigned products, preparing scientific safety analyses, and collaborating with cross-functional teams to determine safety strategies. The role requires in-depth product knowledge and supports the Medical Safety Officer in safety-related activities and documentation.
The Manager, Safety Analysis Scientist role involves leading the safety assessment of assigned products, preparing scientific safety analyses, and collaborating with cross-functional teams to ensure regulatory compliance and inform safety-related decisions. The role requires in-depth product knowledge and supports the Medical Safety Officer in various safety and clinical documentation tasks.
The Manager, Safety Analysis Scientist role involves leading the safety assessment of assigned products, preparing scientific safety analyses, and collaborating with cross-functional teams to determine safety strategies. The role requires in-depth product knowledge and supports the Medical Safety Officer in various safety-related activities.
The Manager, Safety Analysis Scientist role involves leading the safety assessment of assigned products, preparing scientific safety analyses, and collaborating with cross-functional teams to ensure regulatory compliance and inform safety-related decisions. The role requires in-depth product knowledge and supports the Medical Safety Officer in various safety and clinical documentation tasks.
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 on assigned projects, and recommend departmental process improvements.
Leads global strategy and business operations for Johnson & Johnson's Integrated Data Analytics & Reporting (IDAR) function, driving operational excellence, AI-enabled transformation, and financial stewardship across a $500M budget and ~3,000 FTEs. This role shapes the operating model, aligns R&D priorities, and leads a centralized team in finance, vendor management, compliance, and talent strategy to enable scalable, data-driven decision-making across clinical development.
This role involves leading the scientific safety assessment of pharmaceutical products across development and post-marketing stages. The Associate Director will analyze complex medical data, lead safety evaluations, support regulatory submissions, and collaborate with cross-functional teams to shape safety strategies. They will also mentor junior staff, contribute to audits, and drive innovation in safety reporting processes.
This role involves leading the scientific safety assessment of pharmaceutical products across development and post-marketing stages, with a focus on analyzing complex medical data, supporting global safety teams, and contributing to regulatory compliance. The Associate Director acts as a subject matter expert, driving safety strategy, conducting proactive data reviews, and influencing cross-functional decisions. They also lead training, support health authority interactions, and innovate in safety reporting processes.
