Principal Clinical Research Scientist

Role Overview

• Provide scientific and strategic leadership for the design and execution of global clinical studies
• Act as clinical science representative on New Product Development and Core Teams
• Lead the development of clinical study concepts and protocols
• Serve as scientific owner and author of clinical study reports
• Critically review, interpret, and synthesize clinical data
• Establish and maintain strong collaborations with key investigators, KOLs and KEEs
• Represent Radiometer in scientific, clinical, and regulatory forums

Requirements

• Master’s degree in Life Sciences, Healthcare, or a related discipline
• 7+ years of relevant clinical research experience, or a Doctoral degree with 5+ years of experience
• Strong experience with clinical evidence generation for EU and/or US markets
• Solid understanding of clinical study design, execution, and interpretation, including regulatory and scientific expectations
• Experience contributing to FDA regulatory interactions and negotiations related to clinical evidence
• Demonstrated ability to solve complex scientific challenges
• High level of proficiency in scientific writing, critical data review, and interpretation of clinical study results
• Excellent communication and collaboration skills

Benefits

• Health care program
• Paid time off