Position Summary
The Department of Pediatrics (DoP) is seeking a full-time licensed genetic counselor for two innovative projects focused on advancing diagnosis and care for individuals with rare genetic disorders. The position will encompass two roles, one focused on expanded access to clinical and research genomic sequencing, and the second focused on the launch of multidisciplinary clinics for rare genetic disorders.

The DoP is developing an 'on call' genetic counseling clinic aimed at increasing access and reducing wait times for exome and genome sequencing. We are seeking a GC to play a central role in shaping this delivery model and supporting Divisions across the DoP based upon their clinical needs. This role primarily provides pre- and post-test genetic counseling for exome and genome sequencing. The GC in this role would serve as a liaison between patients, families, and the many providers throughout the DoP.

The DoP has also developed six multidisciplinary clinics dedicated to delivering exceptional clinical care for individuals with selected rare genetic disorders. We are seeking a genetic counselor to play a central role in shaping these innovative programs. The successful candidate will lead the development of best-practice standards and oversee centralized tracking of key performance metrics, including family satisfaction measures. This individual will help define patient eligibility criteria, streamline intake and triage processes, and establish standardized procedures for follow-up care. The role also offers opportunities for direct engagement with families-providing education, guidance, and support during clinic sessions as needed as well as involvement in outreach and marketing initiatives in collaboration with patient advocacy organizations.

Key Responsibilities

• Provides genetic counseling to individuals and families at risk for specific hereditary disorders. Interprets family history, clinical and genetic findings to predict risk to patient. Obtains and reviews medical, developmental, and family history information as part of diagnostic team. Ascertains needs and goals of patients/ families.
• Responds to inquiries related to diagnostic evaluations, hereditary risks, genetic testing, and pregnancy exposures. Participates in communication process and educating families. Provides documentation of evaluation for families, referring physicians, and the medical record.
• Collects, tracks and analyses data for both initiatives. Monitors and reviews data/sample collection, computer entry, and related activities to ensure compliance and consistency.
• Oversees and coordinates daily operations of the assigned clinical areas. Acts as liaison between clinical directors, staff, and project collaborators. Contributes to the development of workflows and/or consent forms.
• Responds to inquiries related to eligibility and procedures, diagnostic evaluations, hereditary risks, logistics, and genetic testing within scope of each clinical area.
• Identifies, contacts, and screens potential participants/families for eligibility of participation.
• Obtains informed consent for genetic testing eligible individuals/families. Delivers test results directly to patients/families.
• Develops and participates in genetics education programs for physicians, other health professionals, and lay populations. Trains, supervises, and evaluates graduate-level counseling students.
• Collaborates in developing written documents and web-based materials for a variety of purposes including research protocols, publications and conference presentations.

Minimum Qualifications
Education:

• Master's Degree in Genetic Counseling

Experience:

• Post graduate Genetic Counseling experience preferred

Licensure/ Certifications:

• MA Genetic Counselor License
• Genetic Counselor certification from the American Board of Genetic Counseling or from the American Board of Medical Genetics and Genomics