Your Responsibilities
- 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