Sr Manager Intl Clinical Research

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 our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at jnj.com . As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit. Job Function: Medical Affairs Group Job Sub Function: Medical Affairs Job Category: People Leader All Job Posting Locations: Leeds, West Yorkshire, United Kingdom Job Description: DePuy Synthes is recruiting for a Sr Manager Intl Clinical Research , located in Leeds, UK. The Sr. Manager, International Clinical Research will primarily support local evidence generation, health technology assessment submissions, and dissemination of clinical evidence across international markets, with an initial focus on EMEA. The role will partner with regional business, clinical, regulatory, medical affairs, and commercial stakeholders to ensure locally relevant clinical evidence is generated, interpreted, and communicated effectively to support market access, customer eng agement, and evidence-based decision-making. The role will also consult on clinical regulatory strategy for new product introductions and post-market evidence needs, ensuring alignment with applicable regulatory expectations and global clinical evidence strategy. Key Responsibilities: International Evidence Generation: Lead support for locally relevant evidence generation projects with global impact across international markets, including investigator-initiated studies, collaborative research, registry analyses, and other real-world evidence activities. Work with investigators and internal stakeholders to shape research concepts, assess feasibility, support study set-up, and provide ongoing scientific and operational input through timely meetings and written feedback. Support development or review of study materials, protocols, abstracts, manuscripts, presentations, and medical writing outputs where required . Ensure evidence generation activities are aligned with regional business priorities, clinical evidence gaps, compliance requirements, and available funding pathways. Support local evidence generation projects, including the initiation of investigator-initiated studies. Provide ongoing support for collaborative research projects via timely video conferences or in-person meetings with investigators and or providing medical writing as required . Ensure alignment with business partners with the direction and source funding as appropriate . Clinical Support for Health Technology Assessment and Market Access: Provide clinical and evidence-based support for local health technology assessment submissions, reimbursement activities, value dossiers, and tender responses as required . Interpret clinical evidence in the context of local payer, provider, and customer requirements to support market access and adoption of orthopaedic technologies. Collaborate with regional business partners, health economics and market access colleagues, and commercial teams to ensure evidence messages are accurate , ba lan ced, and aligned with approved claims. Deliver clinical support to local health technology assessments to ensure alignment with product evidence. Provide clinical support to local tenders as required . Dissemination and Translation of Clinical Evidence: Facilitate the local dissemination and translation of clinical evidence into practical resources, including white papers, evidence summaries, training materials, slide content, and customer-facing scientific support materials. Support evidence-focused training for regional sales and commercial teams, including delivery or support of training sessions at Leeds One and other appropriate venues . Support customer-facing evidence discussions, advisory boards, and scientific exchange activities in partnership with medical affairs, professional education, and commercial stakeholders. Support publication and presentation activities at relevant regional and international conferences, including congress abstract development, presentation preparation, and congress evidence p lan ning. Facilitate the local dissemination of clinical evidence, including the development of white papers and training materials to aid sales teams in the utilization of evidence assets. Support local sales training a