Principal Clinical Scientist (Neurodegenerative)

What you’d do

Designs clinical studies and evidence strategies for global regulatory submissions across diagnostic modalities, and serves as scientific liaison with regulators, key opinion leaders, and external sites. Full time; involves cross-functional work with R&D, Regulatory, Medical Affairs, Quality, and Commercial teams, plus mentoring junior scientists. Found on the employer's careers page on Oct 19, 2026. Apply through the link.

You’ll need

• Bachelor's in life sciences or healthcare with 9+ years clinical research experience
• Significant experience in US and/or EU trials
• Clinical study and evidence strategy design
• Regulatory submission experience (FDA 510(k)/PMA, CE-IVDR)
• Clinical and regulatory documentation authoring