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Sign Up to ReadThe Clinical Research Manager defines and owns the clinical evidence strategy for new and updated AI and machine learning algorithms within software‑based digital dentistry solutions. The role ensures that clinical intended use, clinical benefit, and performance claims are clinically and scientifically justified, competitively positioned, and acceptable from a regulatory perspective. The Clinical Research Manager steers clinical research, clarifies the clinical performance specifications for an algorithm based on end-user voice-of-customer, clinical data governance, and clinical validation strategy for AI and machine learning algorithms.
Accountabilities:
Clinical evidence strategy & competitive landscape:
Evaluate and clarify clinical intended use, clinical benefit, and accuracy acceptance criteria at project initiation for new and updated AI and machine learning algorithms
Review scientific literature and existing FDA 510(k) clearances to benchmark claims and validation approaches
Define clinical evidence roadmaps and required clinical validation studies
Clinical data governance & cross-site alignment:
Own clinical data governance across research, training, validation, and regulatory use
Ensure traceability, data integrity, and audit readiness across multiple data collection sites
Collaboration with research & innovation:
Collaborate with research teams on new ideas and early feasibility assessments
Ensure research outputs can be leveraged for downstream validation and regulatory submissions
Clinical validation & regulatory substantiation:
Partner with software validation, quality, and regulatory teams to design clinically meaningful studies
Show deep understanding of clinical validation study methodologies and statistics.
Substantiate clinical claims and study designs using literature and regulatory precedent
Leadership & execution steering:
Act as escalation point for risks related to data quality, study feasibility, and regulatory alignment
Define processes to improve efficiency and effectiveness of clinical evaluations.
Job Requirements:
Hybrid, 4 or more days a week in the office
Envista Holdings Corporation
Office in Belgium
Also hiring in San Jose, United States, United States, Italy and 4 more places
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