Genetic Counselor I

Ann & Robert H. Lurie Children's Hospital of Chicago•Chicago, IL

1d•$76,960 - $125,840•Onsite

About The Position

This is an entry level clinical genetic counselor position providing genetic counseling to patients and families for a variety of indications. The position involves participation in all aspects of delivery of genetics services, including involvement in the diagnostic evaluation process, care coordination, identification of resources, and advocacy. New grads that apply must have completed their program by June of 2026 and include a cover letter. The selected individual will work M-F from the Lurie main hospital campus. The Edwards Family Division of Genetics and Rare Diseases is excited to be recruiting for a new full-time clinical genetic counselor role with primary responsibilities supporting our inpatient consultation service. This is a unique genetic counseling position in a pediatric and general genetics setting providing high level genetics evaluation and genetic counseling during the patient’s admission to our hospital. The person in this role will work alongside 2 genetic counselors currently serving on the inpatient consultation team and partner with our rotating group of metabolic and general genetics physicians and advanced practice providers. The patient population is one of high medical complexity in our neonatal, pediatric, and cardiac intensive care units, and typically require rapid genome sequencing. The ideal candidate will have strengths in flexibility, adaptability, communication, and expertise in interpretation and understanding of clinical exome and genome testing. Come join our growing team of >30 genetic counselors with expertise in a number of subspecialty areas. This is a genetic counselor level I position, and new graduates will be considered for this role.

Requirements

Master’s degree from an accredited genetic counseling graduate program
Active IL Genetic Counselor License
none
Microsoft Office Programs
For research genetic counselors, maintains CITI certifications outlined by IRB to serve as study coordinators

Responsibilities

Proficient in the Core Skills of Genetic Counseling as outline by the National society of Genetic Counselors.
Deep and broad knowledge of genetics.
Ability to tailor, translate and communicate complex information in a simple, relevant way for a broad range of audiences.
Strong interpersonal skills, emotional intelligence and self-awareness.
Ability to dissect and analyze complex problems.
Research skills (self-education).
In-depth knowledge of healthcare delivery.
Performs job functions adhering to Lurie Children’s service principles and mission
Communicates test results to patients/families, referring physicians, primary care physicians and other appropriate clinicians.
Coordinates and communicate all aspects of post evaluation patient follow up.
Writes proper documentation of patient visit and visit letters. Generate other letters for patient case as needed.
Helps coordinate general and specialty genetics clinics as assigned.
Serves as the liaison between specialty services involved in the care of children with genetic disorders and assist with case management of medically complex patients.
Coordinates genetic testing of patient and appropriate family members, including obtaining insurance authorization.
Provides education on the natural history, management, genetics, and inheritance of genetic disorders with language tailored to patients and families.
Performs psychosocial assessment and provides appropriate support and resources to patients and families in the coping of their genetic diagnosis or medical condition.
Participates in inpatient consultations.
Participates in genetic counseling on-call rotation and performs duties such as fielding telephone calls from clinicians and patients requesting genetics information, assessing referrals to Genetics and determining appropriate scheduling of patient, triaging urgent patient calls, etc.
Keeps up to date on latest clinical and research developments in medical genetics.
Masters all necessary functions in Epic or current Lurie Children’s electronic medical record software.
Functions as a liaison between laboratory and clinicians to address questions regarding genetic testing and to help ensure appropriate patient referral.
Screens and reviews orders for genetic tests, whether in-house or sent to reference laboratories. Recommends alternative genetic testing based on analysis of the risk, benefit and cost.
Reviews clinical and family histories as required to outline appropriate genetic testing strategy for ordering clinician.
Provide guidance on obtaining insurance authorization for genetic testing and facilitate the process.
Maintains list of referral testing sites and maintains communication with referral laboratory representatives.
Reviews test results by performing necessary literature searches to integrate new discoveries with clinical diagnoses and test interpretation. Effectively communicate this information to ordering clinicians.
Coordinates appropriate follow up testing with ordering clinicians based on results of the proband and assessment of risk for family members and future pregnancy.
Provides written documentation/reports of test results, summaries, recommendations, and support groups.
Works with laboratory management and clinicians to consolidate genetic reference lab testing on an ongoing basis to minimize the number of laboratories used and negotiate the lowest cost per test.
Assist laboratory revenue cycle coordinator with the establishment of CPT coding for genetic tests to ensure regulatory compliance.
Along with laboratory directors, perform data interpretation and analysis for in house genetic tests, including reviewing relevant patient and family histories to correlate test results.
Generates written documentation/reports of test results and includes disease summaries, recommendations, and support group information.
Communicates genetic test results with appropriate follow up recommendations and facilitates or provides genetic counseling services as requested by healthcare providers.
Performs necessary literature searches to integrate new discoveries with clinical diagnoses and test interpretation.
Participates in molecular laboratory new test development.
Maintain and develop standard operating procedures (SOP) or workflows for optimization of in-house genetic testing interpretation, reporting and curation.
Screens and reviews orders for genetic tests, whether in-house or sent to reference laboratories, and when appropriate, recommend alternative genetic testing approach based on analysis of the risk, benefit and cost.
Assist laboratory revenue cycle coordinator with the establishment of CPT coding for genetic tests to ensure regulatory compliance.
Conducts study start-up activities and prepares and maintains all regulatory documents required by sponsor and/or regulatory agencies.
Prepares protocols, informed consent documents, modifications, renewals, and other necessary documents for review by the IRB and/or sponsor.
Coordinates study activities with other research departments to effectively implement clinical research projects. This includes Obtaining required letters of support and/or approvals as needed (i.e., IBC, SRC, etc.). Monitoring protocols are followed.
Obtains high level of knowledge regarding specific condition(s) which is(are) the subject of the research study to provide education on the natural history, management, genetics, and inheritance of genetic disorders with language tailored to study participants and families.
Identifies, verifies, and recruits eligible study participants and conducts the informed consent/assent process. This includes: Communicating with appropriate clinical team members to identify eligible patients Using functions in Epic such as SlicerDicer to identify eligible patients Attending meetings and patient gatherings to spread awareness of research being conducted at our organization
Performs study participant research visits. This includes: Scheduling necessary study assessments and procedures per study protocol Preparing laboratory/specimen collection kits and ensuring samples are processed and sent out appropriately Communicating with research partners such as CRU, research pharmacy, research laboratory, and other applicable departments regarding study visit Communicating with study participants regarding their study visit so participants understand scheduled study procedures Facilitating travel and reimbursement for study participants if applicable
Conducts site qualification, study initiation, monitoring and/or close-out visits.
Communicates with study sponsor and study vendors and responds to queries/requests promptly.
Records, submits, and maintains study data and documents as outlined in study protocols. This includes: Abstracting data from medical records and enters medical information/data onto protocol specific case report forms, study flow sheets, and other required study forms Preparing abstracted/coded data for processing/analysis Recording data on source documents and CRF’s and/or electronic web-based systems Creating and/or updating case report forms and/or source document templates Maintaining all study documents such as regulatory binders, source documents, correspondence, etc. as required by sponsor and/or regulatory agencies.
Monitors, documents, and reports adverse events as required.
Maintains inventory of research related supplies, lab kits, and equipment.
Functions as a patient liaison and addresses study questions, billing issues, barriers to compliance, etc. and appropriately communicates with study patient’s clinical team as needed.
Assists with QA/QC procedures and QA/QC checks for database validity and data monitoring.
Tracks study progress and deadlines for grants/deliverables.
Attends investigator meetings.
Contributes on the preparation of abstracts/posters for scientific meetings and manuscripts for publication.
Continues to learn new research methods, tools, systems, and scientific principles.
Promotes the ethical conduct of research by actively participating in research related educational meetings/conferences (planning, presenting, etc.).
Adheres to research protocol in compliance with applicable institutional, local and federal regulations (OHRP, FDA, GCP, etc.).
Identifies appropriate research opportunities for patients; and if desired by patients, facilitates patient participation.
For laboratory-based GCs, participates in laboratory research initiatives, including data curation and Precision Medicine initiatives when applicable.
Participate in student education by supervising genetic counseling students and medical students and working with residents, fellows, APN students and nutrition students during their rotation in Genetics.
Provide education to fellow Genetics team members by sharing information from meetings, conferences, journal clubs, and other educational resources.
Provides shadowing opportunities or professional advice to those interested in the genetic counseling field.
For laboratory based GCs, participates in educational activities for referring clinicians, laboratory staff, students, and community healthcare partners on genetic disorders, available genetic tests and general information on genetic test techniques.
Participate in family support, education and patient advocacy programs.
Participate in various Division or Hospital committees, programs or working groups.
Active members of various professional societies such as GTFI, NSGC, ASHG, ACMG, SIMD, etc.

Benefits

Medical, dental and vision insurance
Employer paid group term life and disability
Employer contribution toward Health Savings Account
Flexible Spending Accounts
Paid Time Off (PTO), Paid Holidays and Paid Parental Leave
403(b) with a 5% employer match
Supplemental Life, AD&D and Disability
Critical Illness, Accident and Hospital Indemnity coverage
Tuition assistance
Student loan servicing and support
Adoption benefits
Backup Childcare and Eldercare
Employee Assistance Program, and other specialized behavioral health services and resources for employees and family members
Discount on services at Lurie Children’s facilities
Discount purchasing program