Provide clinical guidance to physicians and healthcare professionals for appropriate test selection
Evaluate clinical indications, phenotypic information and family history to optimize diagnostic yield
Support clinical decision-making prior to sample submission
Participate in clinical discussions with treating physicians when complex diagnostic strategies are required
Act as clinical liaison between laboratory and the treating physician for complex cases
Coordinate clarification requests, phenotypic expansions and additional analyses when required
Support interpretation of complex findings including variants of uncertain significance
Manage expectations regarding turnaround times, limitations and diagnostic outcomes
Support physicians in clinical interpretation of results and their implications for patient management
Participate in genetic counseling support or interconsultation sessions with patients and/or families when applicable and permitted
Assist in the explanation of complex genomic findings, recurrence risks and follow-up strategies
Act as escalation point for challenging or inconclusive diagnostic results
Support reanalysis discussions and long-term case follow-up when clinically justified
Build and maintain strong clinical relationships with physicians, genticists and healthcare institutions
Support case-based clinical discussions focused on patient outcomes rather than product promotion
Collaborate closely with internal teams to ensure seamless clinical experience

Bachelor's degree in Genetcs, Medicine, Biology, Biomedicine or related field with strong clinical-genetics exposure
Experience in clinical genetics diagnostics
Proven involvement in interpretation of complex cases, VUS management and reanalysis
Direct interaction with physicians and/or patients in a clinical genetics context
Experience in laboratory-based or reference diagnostic environments preferred

Medical Science Liaison & Customer Engagement – Diagnostic Genomics

TLDR