Clinical Scientist

Changing lives. Building Careers.

Joining us is a chance to do important work that creates change and shapes the future of healthcare. Thinking differently is what we do best. To us, change equals opportunity. Every day, our colleagues are challenging what’s possible and making headway to innovate new treatment pathways to advance patient outcomes and set new standards of care.

SUMMARY DESCRIPTION The Clinical Scientist supports the planning and execution of clinical evidence programs for products across the Tissue Reconstruction portfolio. This role contributes to study design, protocol development, study execution, data analysis, and interpretation of clinical and real-world data to support regulatory, medical, commercial, and market access objectives.

The scientist works closely with Clinical Development leadership within Medical Affairs and collaborates cross-functionally with downstream Medical Affairs colleagues, as well as Regulatory Affairs, Clinical Operations, Biostatistics, R&D, Marketing, Market Access, and external clinical partners to generate evidence supporting product development, regulatory submissions, clinical claims, scientific communications, reimbursement initiatives, and evidence-based decision-making across the product lifecycle. In addition to traditional clinical studies, the role may contribute to real-world evidence, registry, health economics, outcomes research, and claims-based research initiatives.

The scientist leverages strong analytical and scientific skills to derive insights from diverse data sources and support evidence generation, investigator collaborations, and scientific publications that advance patient care and product adoption.

SUPERVISION RECEIVED Reports to Medical Strategy Lead SUPERVISION EXERCISEDNoneKEY RESPONSIBILITIES Contribute to the development and execution of clinical evidence strategies supporting products across the Tissue Reconstruction portfolio.

Conduct literature reviews, evidence gap assessments, and scientific landscape analyses to inform evidence-generation priorities.

Lead the scientific design of assigned studies and contribute to the development of protocols, data collection instruments, analysis plans, and study reports in collaboration with Clinical Operations, Medical Communications, and Biostatistics.

Design, plan, and execute clinical studies, registries, real-world evidence, outcomes research, and claims-based research initiatives.

Lead assigned study and evidence-generation work streams with accountability for timelines, deliverables, study quality, and execution.

Analyze, interpret, and synthesize clinical, real-world, health economics, and published data to generate scientific insights regarding evidence gaps, competitive evidence evaluations, and landscape analyses to inform clinical development and evidence strategy.

Contribute to scientific publications, conference presentations, and other evidence dissemination activities.

Present scientific findings and evidence-based recommendations to internal stakeholders and cross-functional teams.

Collaborate with Medical Affairs, Regulatory Affairs, Clinical Operations, Biostatistics, R&D, Marketing, Market Access, and external investigators to align evidence-generation activities with product development and business needs.

Support investigator and KOL collaborations through study planning discussions, advisory activities, and investigator-initiated research programs.

DESIRED MINIMUM QUALIFICATIONS Advanced degree required (Master's minimum; Ph.D. preferred) in Biomedical Engineering, Biomaterials, Tissue Engineering, Regenerative Medicine, Biological Sciences, Public Health, Epidemiology, Health Outcomes Research, or a related scientific discipline.

Minimum of 3 years of…