Genetic Counselor I, Oncology

Posted:
12/9/2024, 3:13:30 AM

Location(s):
Chicago, Illinois, United States ⋅ Illinois, United States

Experience Level(s):
Junior ⋅ Mid Level

Field(s):
Medical, Clinical & Veterinary

Ann & Robert H. Lurie Children’s Hospital of Chicago provides superior pediatric care in a setting that offers the latest benefits and innovations in medical technology, research and family-friendly design. As the largest pediatric provider in the region with a 140-year legacy of excellence, kids and their families are at the center of all we do. Ann & Robert H. Lurie Children’s Hospital of Chicago is ranked in all 10 specialties by the U.S. News & World Report.

Location

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

Job Description

Essential Job Functions:

Core Responsibilities for all Genetic Counselors:

  • 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 core values and mission

The following list of responsibilities may or may not be applicable based on your individual position and job responsibilities.

Clinical Genetic Counselor Responsibilities:

  • 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 if applicable.

  • Participates in genetic counseling on-call rotation if applicable 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.

  • Serves as a lead coordinator for multidisciplinary and/or specialty clinic, including organizing clinic schedule, communicating with participating groups, lead projects to continue clinic growth and serve more patients, and improve delivery of clinic services.

  • Becomes recognized as expert in specific area of genetics or specific genetic disorder by providing presentations, participating in ad board meetings and participating in multicenter or large scale research projects.

  • Participates in a Division level improvement project that will benefit patient care and services, such as streamlining insurance authorization process, improving clinic documentation, improving communication with patients, etc.

  • Other responsibilities as they arise that are within the genetic counselor’s scope of practice.

Laboratory Utilization Management Genetic Counselor Responsibilities:

  • 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.

  • Leads and facilitates communication between laboratory team and genetic genetics team regarding changes to laboratory services and processes.

  • Participates in a Genetics Laboratory/Pathology improvement project that will benefit patient care and services.

  • Becomes recognized as expert as a molecular genetics or lab utilization management genetic counselor by providing presentations, participating in ad board meetings and participating in multicenter or large scale research projects.

  • Other responsibilities as they arise that are within the genetic counselor’s scope of practice.

Molecular Laboratory Genetic Counselor Responsibilities:

  • 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.

  • Leads and facilitates communication between laboratory team and genetic genetics team regarding changes to laboratory services and processes.

  • Participates in a Genetics Laboratory/Pathology improvement project that will benefit patient care and services.

  • Becomes recognized as expert as a molecular genetics or lab utilization management genetic counselor by providing presentations, participating in ad board meetings and participating in multicenter or large scale research projects.. 

  • Other responsibilities as they arise that are within the genetic counselor’s scope of practice.

Research Genetic Counselor Responsibilities:

  • 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 patients 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

  • Manges and 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. Educates participants on continued investigational product (IP) compliance.

  • Helps research staff and study participants understand and recognize the difference between research related activities and assessments, and participants ongoing clinical care and management needs of their condition.

  • Assists with QA/QC procedures and QA/QC checks for database validity and data monitoring.

  • Tracks study progress and deadlines for grants/deliverables.

  • Perform financial tasks related to studies, which include:

    • Assisting in the preparation of budgets and fund management.

    • Preparing study invoices and study billing.

  • Evaluates new protocols for feasibility.

  • Assists in the training of personnel for role in study conduct; maintains delegation of authority and training logs.

  • Assists in statistical analysis in research studies under guidance of statistician.

  • Prepares for and facilitates external audits by sponsor, regulatory agencies (OHRP, FDA, etc.).

  • Attends investigator meetings.

  • Participates in the production of abstracts/posters for scientific meetings and manuscripts for publication as a contributing or lead author; and presents research data at national scientific meetings.

  • Assists the PI in drafting investigator led research protocols, grant submissions, and grant reports.

  • Assists in the submission of required documents to regulatory authorities (i.e., FDA) when applicable.

  • Registers study with clinicaltrails.gov if applicable.

  • Participates in process improvement projects for clinical research studies, and research workflows at the division and institutional levels.

  • Serves on relevant research committees.

  • Continues to learn new research methods, tools, systems, and scientific principles and shares knowledge with others.

  • Serves as a resource for other research genetic counselors and clinical research coordinators. Assists in the onboarding and training of new hires, which can include serving as a preceptor.

  • 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.).

  • Other responsibilities as they arise that are within the genetic counselor’s scope of practice.

Research Activities not associated with Research Genetic Counselor Responsibilities:

  • Participates in a research project at Lurie Children’s or in collaboration with other institutions.  If enrolled as study personnel in IRB approved study, comply with IRB standards and maintain Human Subjects and Good Clinical Practice certifications.

  • When opportunities arise, participates in student research project by serving on student thesis committee.

  • Participates in authorship or is lead author of abstract submitted to major genetics or other scientific educational meeting or conference.

Education Activities:

  • Provides lectures or participates in student courses, workshops or other educational programs at Feinberg School or Medicine, Northwestern University Graduate Program in Genetic Counseling or other educational institutions.

  • Participates in educational events for health care providers within Lurie Children’s or the community.

  • Serves as lead supervisor for student rotation.

Advocacy Activities:

  • Participates in the organization of patient advocacy or patient education meeting.

  • Participates in promotion of genetic counselor activities and awareness within Lurie Children’s and greater community.

Leadership and Professional Development Activities:

  • Serves as Committee Chair/leader in a Division or Hospital committee.

  • Participates on a committee or program activities in one of the major professional societies such as GTFI, NSGC, ASHG, ACMG, SIMD.

  • Serves as a preceptor for new hired and less experienced genetic counselors.

  • Serves as a mentor for Level I Genetic Counselors

Knowledge, Skills and Abilities:

  • Education: Master’s degree from an accredited genetic counseling graduate program

  • Certification/Licensure/Registration: Active IL Genetic Counseling License

  • Years of Relevant Experience: minimum of 2 years

  • For research genetic counselors, maintains CITI certifications outlined by IRB to serve as study coordinators

  • Computer Skills (i.e. Software/Hardware): Microsoft Office Programs

  • Other Skills (i.e. Project Management, Negotiation)

Education

Benefit Statement

For full time and part time employees who work 20 or more hours per week we offer a generous benefits package that includes:

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

Various voluntary benefits:

  • 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

There’s a Place for You with Us

At Lurie Children’s we embrace and celebrate diversity and equity in a serious way. We are committed to building a team with a variety of backgrounds, skills, and viewpoints — recognizing that diverse identities strengthen our workplace and the care we can provide to the Chicago community and beyond. We treat everyone fairly, appreciate differences, and make meaningful connections that foster belonging and allyship. This is a place where you can be your best, so we can give our best to the patients and families who trust us with their care.  

Lurie Children’s and its affiliates are equal employment opportunity employers.  We value diversity and are committed to creating an inclusive environment for all employees.  All qualified applicants will receive consideration for employment without regard to race, color, sex, sexual orientation, gender identity or expression, religion, national origin, ancestry, age, disability, marital status, pregnancy, protected veteran status, order of protection status, protected genetic information, or any other characteristic protected by law.

Support email: [email protected]

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

Website: https://luriechildrens.org/

Headquarter Location: Chicago, Illinois, United States

Employee Count: 1001-5000

Year Founded: 1900

IPO Status: Private

Last Funding Type: Grant

Industries: Children ⋅ Health Care ⋅ Hospital ⋅ Medical