Clinical Scientist, Tissue Reconstruction Evidence

Integra LifeSciences; United States; Remote; USD 82,000 - 113,000; Full time

Job summary

Integra LifeSciences is seeking a Clinical Scientist to lead the planning and execution of clinical evidence programs within the Tissue Reconstruction portfolio. You will design studies, develop protocols, analyze data, and contribute to regulatory, medical, and market access objectives, collaborating across Clinical Operations, Biostatistics, R&D, and Regulatory Affairs.

You will leverage real-world evidence, literature reviews, and health economics research to generate insights that

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 related field.
• Minimum of 3 years of relevant experience in clinical development, clinical research, medical affairs, epidemiology, health outcomes, real-world evidence, or related evidence-generation functions.
• Experience supporting clinical studies, registries, real-world evidence, outcomes research, health economics, or claims-based research preferred.

Responsibilities

• Contribute to the development and execution of clinical evidence strategies across Tissue Reconstruction products.
• Lead literature reviews, evidence gap assessments, and landscape analyses to inform priorities.
• Design, plan, and execute clinical studies, registries, and real-world evidence initiatives.

Skills

Analytical reasoning

Scientific writing

Communication skills

Cross-functional collaboration

Project management

Statistical interpretation

Education

Master’s degree (minimum)

PhD preferred

Tools

Excel

R

SAS

SQL

Power BI

Tableau

Job description

Integra LifeSciences is seeking a Clinical Scientist to lead the planning and execution of clinical evidence programs within the Tissue Reconstruction portfolio. You will design studies, develop protocols, analyze data, and contribute to regulatory, medical, and market access objectives, collaborating across Clinical Operations, Biostatistics, R&D, and Regulatory Affairs.

You will leverage real-world evidence, literature reviews, and health economics research to generate insights that